Canonical Allele Identifier: CA2702244317

Gene: TRAK1

Linked Data

• dbSNP Id: rs766037909

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42210117_42210118insAGGAAG , CM000665.2:g.42210117_42210118insAGGAAG	GRCh38
NC_000003.11:g.42251609_42251610insAGGAAG , CM000665.1:g.42251609_42251610insAGGAAG	GRCh37
NC_000003.10:g.42226613_42226614insAGGAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327628.10:c.1963+132_1963+133insAGGAAG MANE Select	ENSP00000328998.5:n.1963+132_1963+133insAGGAAG
ENST00000672026.1:c.1651+132_1651+133insAGGAAG	ENSP00000500099.1:n.1651+132_1651+133insAGGAAG
ENST00000673621.2:c.2047+132_2047+133insAGGAAG	ENSP00000500819.2:n.2047+132_2047+133insAGGAAG
ENST00000327628.9:c.1963+132_1963+133insAGGAAG	ENSP00000328998.5:n.1963+132_1963+133insAGGAAG
ENST00000341421.7:c.1921_1922insAGGAAG	ENSP00000340702.3:p.Glu640_Gly641insGluGlu
ENST00000396175.5:c.1789+132_1789+133insAGGAAG	ENSP00000379478.1:n.1789+132_1789+133insAGGAAG
ENST00000487159.5:c.1651+132_1651+133insAGGAAG	ENSP00000486713.1:n.1651+132_1651+133insAGGAAG
ENST00000613405.4:c.1873_1874insAGGAAG	ENSP00000483516.1:p.Glu624_Gly625insGluGlu
NM_001042646.2:c.1963+132_1963+133insAGGAAG	NP_001036111.1:n.1963+132_1963+133insAGGAAG
NM_001265608.1:c.2095_2096insAGGAAG	NP_001252537.1:p.Glu698_Gly699insGluGlu
NM_001265609.1:c.1873_1874insAGGAAG	NP_001252538.1:p.Glu624_Gly625insGluGlu
NM_014965.4:c.1921_1922insAGGAAG	NP_055780.2:p.Glu640_Gly641insGluGlu
XM_005264956.2:c.1900+195_1900+196insAGGAAG	XP_005265013.1:n.1900+195_1900+196insAGGAAG
XM_005264957.2:c.1789+132_1789+133insAGGAAG	XP_005265014.1:n.1789+132_1789+133insAGGAAG
XM_005264958.2:c.1741+132_1741+133insAGGAAG	XP_005265015.1:n.1741+132_1741+133insAGGAAG
XM_005264959.2:c.1651+132_1651+133insAGGAAG	XP_005265016.1:n.1651+132_1651+133insAGGAAG
XM_005264960.2:c.1963+132_1963+133insAGGAAG	XP_005265017.1:n.1963+132_1963+133insAGGAAG
XM_005264962.3:c.1963+132_1963+133insAGGAAG	XP_005265019.1:n.1963+132_1963+133insAGGAAG
XM_005264963.3:c.1900+195_1900+196insAGGAAG	XP_005265020.1:n.1900+195_1900+196insAGGAAG
XM_006713028.2:c.1900+195_1900+196insAGGAAG	XP_006713091.1:n.1900+195_1900+196insAGGAAG
XM_006713029.2:c.1963+132_1963+133insAGGAAG	XP_006713092.1:n.1963+132_1963+133insAGGAAG
XM_006713030.2:c.1900+195_1900+196insAGGAAG	XP_006713093.1:n.1900+195_1900+196insAGGAAG
XM_006713031.2:c.1900+195_1900+196insAGGAAG	XP_006713094.1:n.1900+195_1900+196insAGGAAG
XM_011533487.1:c.2032+132_2032+133insAGGAAG	XP_011531789.1:n.2032+132_2032+133insAGGAAG
XM_011533488.1:c.1963+132_1963+133insAGGAAG	XP_011531790.1:n.1963+132_1963+133insAGGAAG
XM_011533489.1:c.1963+132_1963+133insAGGAAG	XP_011531791.1:n.1963+132_1963+133insAGGAAG
NM_001349245.1:c.1588+195_1588+196insAGGAAG	NP_001336174.1:n.1588+195_1588+196insAGGAAG
NM_001349246.1:c.1900+195_1900+196insAGGAAG	NP_001336175.1:n.1900+195_1900+196insAGGAAG
NM_001349247.1:c.1963+132_1963+133insAGGAAG	NP_001336176.1:n.1963+132_1963+133insAGGAAG
NM_001349248.1:c.1678+195_1678+196insAGGAAG	NP_001336177.1:n.1678+195_1678+196insAGGAAG
NM_001349249.1:c.1741+132_1741+133insAGGAAG	NP_001336178.1:n.1741+132_1741+133insAGGAAG
NR_146089.1:n.2010+195_2010+196insAGGAAG
XM_005264962.4:c.1963+132_1963+133insAGGAAG	XP_005265019.1:n.1963+132_1963+133insAGGAAG
XM_005264963.4:c.1900+195_1900+196insAGGAAG	XP_005265020.1:n.1900+195_1900+196insAGGAAG
XM_006713029.3:c.1963+132_1963+133insAGGAAG	XP_006713092.1:n.1963+132_1963+133insAGGAAG
XM_006713030.3:c.1900+195_1900+196insAGGAAG	XP_006713093.1:n.1900+195_1900+196insAGGAAG
XM_006713031.4:c.1900+195_1900+196insAGGAAG	XP_006713094.1:n.1900+195_1900+196insAGGAAG
XM_011533489.3:c.1963+132_1963+133insAGGAAG	XP_011531791.1:n.1963+132_1963+133insAGGAAG
XM_017005906.1:c.2164_2165insAGGAAG	XP_016861395.1:p.Glu721_Gly722insGluGlu
XM_017005907.2:c.1921_1922insAGGAAG	XP_016861396.1:p.Glu640_Gly641insGluGlu
XM_017005908.1:c.1873_1874insAGGAAG	XP_016861397.1:p.Glu624_Gly625insGluGlu
XM_017005909.1:c.1783_1784insAGGAAG	XP_016861398.1:p.Glu594_Gly595insGluGlu
XM_017005911.1:c.1588+195_1588+196insAGGAAG	XP_016861400.1:n.1588+195_1588+196insAGGAAG
XM_017005913.2:c.1900+195_1900+196insAGGAAG	XP_016861402.1:n.1900+195_1900+196insAGGAAG
XM_024453400.1:c.2095_2096insAGGAAG	XP_024309168.1:p.Glu698_Gly699insGluGlu
XM_024453401.1:c.2095_2096insAGGAAG	XP_024309169.1:p.Glu698_Gly699insGluGlu
XM_024453402.1:c.1963+132_1963+133insAGGAAG	XP_024309170.1:n.1963+132_1963+133insAGGAAG
XM_024453403.1:c.1900+195_1900+196insAGGAAG	XP_024309171.1:n.1900+195_1900+196insAGGAAG
XM_024453404.1:c.1963+132_1963+133insAGGAAG	XP_024309172.1:n.1963+132_1963+133insAGGAAG
XR_001740058.2:n.2017+132_2017+133insAGGAAG
XR_001740059.2:n.1954+195_1954+196insAGGAAG
XR_001740060.1:n.2422+195_2422+196insAGGAAG
NM_001042646.3:c.1963+132_1963+133insAGGAAG MANE Select	NP_001036111.1:n.1963+132_1963+133insAGGAAG
NM_001265608.2:c.2095_2096insAGGAAG	NP_001252537.1:p.Glu698_Gly699insGluGlu
NM_001349246.2:c.1900+195_1900+196insAGGAAG	NP_001336175.1:n.1900+195_1900+196insAGGAAG
NM_001349247.2:c.1963+132_1963+133insAGGAAG	NP_001336176.1:n.1963+132_1963+133insAGGAAG
NM_014965.5:c.1921_1922insAGGAAG	NP_055780.2:p.Glu640_Gly641insGluGlu
NM_001265609.2:c.1873_1874insAGGAAG	NP_001252538.1:p.Glu624_Gly625insGluGlu