Canonical Allele Identifier: CA445963183

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174405T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838708T>G , CM000667.2:g.112838708T>G	GRCh38
NC_000005.9:g.112174405T>G , CM000667.1:g.112174405T>G	GRCh37
NC_000005.8:g.112202304T>G	NCBI36
NG_008481.4:g.151188T>G , LRG_130:g.151188T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2779T>G	ENSP00000484935.2:n.2779T>G
ENST00000504915.3:c.3168T>G	ENSP00000473355.2:p.Ser1056=
ENST00000505350.2:c.*3120T>G	ENSP00000481752.1:n.*3120T>G
ENST00000507379.6:c.3060T>G	ENSP00000423224.2:p.Ser1020=
ENST00000509732.6:c.3114T>G	ENSP00000426541.2:p.Ser1038=
ENST00000512211.7:c.3114T>G	ENSP00000423828.3:p.Ser1038=
ENST00000257430.9:c.3114T>G MANE Select	ENSP00000257430.4:p.Ser1038=
ENST00000257430.8:c.3114T>G	ENSP00000257430.4:p.Ser1038=
ENST00000502371.2:c.1467T>G
ENST00000507379.5:c.3060T>G	ENSP00000423224.1:p.Ser1020=
ENST00000508376.6:c.3114T>G	ENSP00000427089.2:p.Ser1038=
ENST00000508624.5:c.*2436T>G	ENSP00000424265.1:n.*2436T>G
ENST00000512211.6:c.3114T>G	ENSP00000423828.2:p.Ser1038=
ENST00000520401.1:c.230+9736T>G
NM_000038.5:c.3114T>G	NP_000029.2:p.Ser1038=
NM_001127510.2:c.3114T>G	NP_001120982.1:p.Ser1038=
NM_001127511.2:c.3060T>G	NP_001120983.2:p.Ser1020=
NM_001354895.1:c.3114T>G	NP_001341824.1:p.Ser1038=
NM_001354896.1:c.3168T>G	NP_001341825.1:p.Ser1056=
NM_001354897.1:c.3144T>G	NP_001341826.1:p.Ser1048=
NM_001354898.1:c.3039T>G	NP_001341827.1:p.Ser1013=
NM_001354899.1:c.3030T>G	NP_001341828.1:p.Ser1010=
NM_001354900.1:c.2991T>G	NP_001341829.1:p.Ser997=
NM_001354901.1:c.2937T>G	NP_001341830.1:p.Ser979=
NM_001354902.1:c.2841T>G	NP_001341831.1:p.Ser947=
NM_001354903.1:c.2811T>G	NP_001341832.1:p.Ser937=
NM_001354904.1:c.2736T>G	NP_001341833.1:p.Ser912=
NM_001354905.1:c.2634T>G	NP_001341834.1:p.Ser878=
NM_001354906.1:c.2265T>G	NP_001341835.1:p.Ser755=
NM_000038.6:c.3114T>G MANE Select	NP_000029.2:p.Ser1038=
NM_001127510.3:c.3114T>G	NP_001120982.1:p.Ser1038=
NM_001127511.3:c.3060T>G	NP_001120983.2:p.Ser1020=
NM_001354895.2:c.3114T>G	NP_001341824.1:p.Ser1038=
NM_001354896.2:c.3168T>G	NP_001341825.1:p.Ser1056=
NM_001354897.2:c.3144T>G	NP_001341826.1:p.Ser1048=
NM_001354898.2:c.3039T>G	NP_001341827.1:p.Ser1013=
NM_001354899.2:c.3030T>G	NP_001341828.1:p.Ser1010=
NM_001354900.2:c.2991T>G	NP_001341829.1:p.Ser997=
NM_001354901.2:c.2937T>G	NP_001341830.1:p.Ser979=
NM_001354902.2:c.2841T>G	NP_001341831.1:p.Ser947=
NM_001354903.2:c.2811T>G	NP_001341832.1:p.Ser937=
NM_001354904.2:c.2736T>G	NP_001341833.1:p.Ser912=
NM_001354905.2:c.2634T>G	NP_001341834.1:p.Ser878=
NM_001354906.2:c.2265T>G	NP_001341835.1:p.Ser755=