Canonical Allele Identifier: CA16025186

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112170674T>G (hg19) ; chr5:g.112834977T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112834977T>G , CM000667.2:g.112834977T>G	GRCh38
NC_000005.9:g.112170674T>G , CM000667.1:g.112170674T>G	GRCh37
NC_000005.8:g.112198573T>G	NCBI36
NG_008481.4:g.147457T>G , LRG_130:g.147457T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1435T>G	ENSP00000484935.2:p.Cys479Gly
ENST00000504915.3:c.1824T>G	ENSP00000473355.2:p.Ser608Arg
ENST00000505350.2:c.*1776T>G	ENSP00000481752.1:n.*1776T>G
ENST00000507379.6:c.1716T>G	ENSP00000423224.2:p.Ser572Arg
ENST00000509732.6:c.1770T>G	ENSP00000426541.2:p.Ser590Arg
ENST00000512211.7:c.1770T>G	ENSP00000423828.3:p.Ser590Arg
ENST00000257430.9:c.1770T>G MANE Select	ENSP00000257430.4:p.Ser590Arg
ENST00000257430.8:c.1770T>G	ENSP00000257430.4:p.Ser590Arg
ENST00000502371.2:c.123T>G
ENST00000504915.2:c.459T>G	ENSP00000473355.1:p.Ser153Arg
ENST00000507379.5:c.1716T>G	ENSP00000423224.1:p.Ser572Arg
ENST00000508376.6:c.1770T>G	ENSP00000427089.2:p.Ser590Arg
ENST00000508624.5:c.*1092T>G	ENSP00000424265.1:n.*1092T>G
ENST00000512211.6:c.1770T>G	ENSP00000423828.2:p.Ser590Arg
ENST00000520401.1:c.230+6005T>G
NM_000038.5:c.1770T>G	NP_000029.2:p.Ser590Arg
NM_001127510.2:c.1770T>G	NP_001120982.1:p.Ser590Arg
NM_001127511.2:c.1716T>G	NP_001120983.2:p.Ser572Arg
NM_001354895.1:c.1770T>G	NP_001341824.1:p.Ser590Arg
NM_001354896.1:c.1824T>G	NP_001341825.1:p.Ser608Arg
NM_001354897.1:c.1800T>G	NP_001341826.1:p.Ser600Arg
NM_001354898.1:c.1695T>G	NP_001341827.1:p.Ser565Arg
NM_001354899.1:c.1686T>G	NP_001341828.1:p.Ser562Arg
NM_001354900.1:c.1647T>G	NP_001341829.1:p.Ser549Arg
NM_001354901.1:c.1593T>G	NP_001341830.1:p.Ser531Arg
NM_001354902.1:c.1497T>G	NP_001341831.1:p.Ser499Arg
NM_001354903.1:c.1467T>G	NP_001341832.1:p.Ser489Arg
NM_001354904.1:c.1392T>G	NP_001341833.1:p.Ser464Arg
NM_001354905.1:c.1290T>G	NP_001341834.1:p.Ser430Arg
NM_001354906.1:c.921T>G	NP_001341835.1:p.Ser307Arg
NM_000038.6:c.1770T>G MANE Select	NP_000029.2:p.Ser590Arg
NM_001127510.3:c.1770T>G	NP_001120982.1:p.Ser590Arg
NM_001127511.3:c.1716T>G	NP_001120983.2:p.Ser572Arg
NM_001354895.2:c.1770T>G	NP_001341824.1:p.Ser590Arg
NM_001354896.2:c.1824T>G	NP_001341825.1:p.Ser608Arg
NM_001354897.2:c.1800T>G	NP_001341826.1:p.Ser600Arg
NM_001354898.2:c.1695T>G	NP_001341827.1:p.Ser565Arg
NM_001354899.2:c.1686T>G	NP_001341828.1:p.Ser562Arg
NM_001354900.2:c.1647T>G	NP_001341829.1:p.Ser549Arg
NM_001354901.2:c.1593T>G	NP_001341830.1:p.Ser531Arg
NM_001354902.2:c.1497T>G	NP_001341831.1:p.Ser499Arg
NM_001354903.2:c.1467T>G	NP_001341832.1:p.Ser489Arg
NM_001354904.2:c.1392T>G	NP_001341833.1:p.Ser464Arg
NM_001354905.2:c.1290T>G	NP_001341834.1:p.Ser430Arg
NM_001354906.2:c.921T>G	NP_001341835.1:p.Ser307Arg