Canonical Allele Identifier: CA10582321

Gene: APC

Linked Data

• ClinVar Variation Id: 236611
• ClinVar RCV Id: RCV002229613 ; RCV003337263
• dbSNP Id: rs758987855
• COSMIC: COSM6475415
• MyVariant Identifiers: chr5:g.112176278G>T (hg19) ; chr5:g.112840581G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840581G>T , CM000667.2:g.112840581G>T	GRCh38
NC_000005.9:g.112176278G>T , CM000667.1:g.112176278G>T	GRCh37
NC_000005.8:g.112204177G>T	NCBI36
NG_008481.4:g.153061G>T , LRG_130:g.153061G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5041G>T	ENSP00000473355.2:p.Glu1681Ter
ENST00000505350.2:c.*4993G>T	ENSP00000481752.1:n.*4993G>T
ENST00000507379.6:c.4933G>T	ENSP00000423224.2:p.Glu1645Ter
ENST00000509732.6:c.4987G>T	ENSP00000426541.2:p.Glu1663Ter
ENST00000512211.7:c.4987G>T	ENSP00000423828.3:p.Glu1663Ter
ENST00000257430.9:c.4987G>T MANE Select	ENSP00000257430.4:p.Glu1663Ter
ENST00000257430.8:c.4987G>T	ENSP00000257430.4:p.Glu1663Ter
ENST00000508376.6:c.4987G>T	ENSP00000427089.2:p.Glu1663Ter
ENST00000508624.5:c.*4309G>T	ENSP00000424265.1:n.*4309G>T
ENST00000520401.1:c.230+11609G>T
NM_000038.5:c.4987G>T	NP_000029.2:p.Glu1663Ter
NM_001127510.2:c.4987G>T	NP_001120982.1:p.Glu1663Ter
NM_001127511.2:c.4933G>T	NP_001120983.2:p.Glu1645Ter
NM_001354895.1:c.4987G>T	NP_001341824.1:p.Glu1663Ter
NM_001354896.1:c.5041G>T	NP_001341825.1:p.Glu1681Ter
NM_001354897.1:c.5017G>T	NP_001341826.1:p.Glu1673Ter
NM_001354898.1:c.4912G>T	NP_001341827.1:p.Glu1638Ter
NM_001354899.1:c.4903G>T	NP_001341828.1:p.Glu1635Ter
NM_001354900.1:c.4864G>T	NP_001341829.1:p.Glu1622Ter
NM_001354901.1:c.4810G>T	NP_001341830.1:p.Glu1604Ter
NM_001354902.1:c.4714G>T	NP_001341831.1:p.Glu1572Ter
NM_001354903.1:c.4684G>T	NP_001341832.1:p.Glu1562Ter
NM_001354904.1:c.4609G>T	NP_001341833.1:p.Glu1537Ter
NM_001354905.1:c.4507G>T	NP_001341834.1:p.Glu1503Ter
NM_001354906.1:c.4138G>T	NP_001341835.1:p.Glu1380Ter
NM_000038.6:c.4987G>T MANE Select	NP_000029.2:p.Glu1663Ter
NM_001127510.3:c.4987G>T	NP_001120982.1:p.Glu1663Ter
NM_001127511.3:c.4933G>T	NP_001120983.2:p.Glu1645Ter
NM_001354895.2:c.4987G>T	NP_001341824.1:p.Glu1663Ter
NM_001354896.2:c.5041G>T	NP_001341825.1:p.Glu1681Ter
NM_001354897.2:c.5017G>T	NP_001341826.1:p.Glu1673Ter
NM_001354898.2:c.4912G>T	NP_001341827.1:p.Glu1638Ter
NM_001354899.2:c.4903G>T	NP_001341828.1:p.Glu1635Ter
NM_001354900.2:c.4864G>T	NP_001341829.1:p.Glu1622Ter
NM_001354901.2:c.4810G>T	NP_001341830.1:p.Glu1604Ter
NM_001354902.2:c.4714G>T	NP_001341831.1:p.Glu1572Ter
NM_001354903.2:c.4684G>T	NP_001341832.1:p.Glu1562Ter
NM_001354904.2:c.4609G>T	NP_001341833.1:p.Glu1537Ter
NM_001354905.2:c.4507G>T	NP_001341834.1:p.Glu1503Ter
NM_001354906.2:c.4138G>T	NP_001341835.1:p.Glu1380Ter