Canonical Allele Identifier: CA357972128

Gene: TBCK

Linked Data

• MyVariant Identifiers: chr4:g.107037470G>C (hg19) ; chr4:g.106116313G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.106116313G>C , CM000666.2:g.106116313G>C	GRCh38
NC_000004.11:g.107037470G>C , CM000666.1:g.107037470G>C	GRCh37
NC_000004.10:g.107256919G>C	NCBI36
NG_034057.2:g.210183C>G
NG_034057.3:g.205371C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273980.10:c.2301C>G	ENSP00000273980.4:p.Asp767Glu
ENST00000394708.7:c.2301C>G MANE Select	ENSP00000378198.2:p.Asp767Glu
ENST00000273980.9:c.2301C>G	ENSP00000273980.4:p.Asp767Glu
ENST00000361687.8:c.2112C>G	ENSP00000355338.4:p.Asp704Glu
ENST00000394706.7:c.2184C>G	ENSP00000378196.3:p.Asp728Glu
ENST00000394708.6:c.2301C>G	ENSP00000378198.2:p.Asp767Glu
ENST00000432496.6:c.2301C>G	ENSP00000405847.2:p.Asp767Glu
ENST00000467183.6:c.*1940C>G	ENSP00000421182.1:n.*1940C>G
ENST00000510927.5:n.1954C>G
ENST00000514689.5:n.593C>G
NM_001163435.2:c.2301C>G	NP_001156907.1:p.Asp767Glu
NM_001163436.2:c.2301C>G	NP_001156908.1:p.Asp767Glu
NM_001163437.2:c.2184C>G	NP_001156909.1:p.Asp728Glu
NM_001290768.1:c.1785C>G	NP_001277697.1:p.Asp595Glu
NM_033115.4:c.2112C>G	NP_149106.2:p.Asp704Glu
XM_011532417.1:c.2301C>G	XP_011530719.1:p.Asp767Glu
XM_011532418.1:c.1983C>G	XP_011530720.1:p.Asp661Glu
XM_011532419.1:c.1785C>G	XP_011530721.1:p.Asp595Glu
XM_011532417.2:c.2301C>G	XP_011530719.1:p.Asp767Glu
XM_017008846.1:c.2301C>G	XP_016864335.1:p.Asp767Glu
XM_017008847.2:c.2301C>G	XP_016864336.1:p.Asp767Glu
XM_017008848.1:c.1983C>G	XP_016864337.1:p.Asp661Glu
XM_017008849.1:c.1785C>G	XP_016864338.1:p.Asp595Glu
XM_024454281.1:c.2301C>G	XP_024310049.1:p.Asp767Glu
XM_024454282.1:c.2301C>G	XP_024310050.1:p.Asp767Glu
XR_002959772.1:n.2495C>G
NM_001163435.3:c.2301C>G MANE Select	NP_001156907.2:p.Asp767Glu
NM_001163436.4:c.2301C>G	NP_001156908.2:p.Asp767Glu
NM_001163437.3:c.2184C>G	NP_001156909.2:p.Asp728Glu
NM_001290768.2:c.1785C>G	NP_001277697.2:p.Asp595Glu
NM_033115.5:c.2112C>G	NP_149106.3:p.Asp704Glu