Canonical Allele Identifier: CA16031568

Gene: APC

Linked Data

• ClinVar Variation Id: 489456
• ClinVar RCV Id: RCV000579761 ; RCV004001227
• dbSNP Id: rs769121879
• MyVariant Identifiers: chr5:g.112175961T>A (hg19) ; chr5:g.112840264T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840264T>A , CM000667.2:g.112840264T>A	GRCh38
NC_000005.9:g.112175961T>A , CM000667.1:g.112175961T>A	GRCh37
NC_000005.8:g.112203860T>A	NCBI36
NG_008481.4:g.152744T>A , LRG_130:g.152744T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4724T>A	ENSP00000473355.2:p.Ile1575Asn
ENST00000505350.2:c.*4676T>A	ENSP00000481752.1:n.*4676T>A
ENST00000507379.6:c.4616T>A	ENSP00000423224.2:p.Ile1539Asn
ENST00000509732.6:c.4670T>A	ENSP00000426541.2:p.Ile1557Asn
ENST00000512211.7:c.4670T>A	ENSP00000423828.3:p.Ile1557Asn
ENST00000257430.9:c.4670T>A MANE Select	ENSP00000257430.4:p.Ile1557Asn
ENST00000257430.8:c.4670T>A	ENSP00000257430.4:p.Ile1557Asn
ENST00000508376.6:c.4670T>A	ENSP00000427089.2:p.Ile1557Asn
ENST00000508624.5:c.*3992T>A	ENSP00000424265.1:n.*3992T>A
ENST00000520401.1:c.230+11292T>A
NM_000038.5:c.4670T>A	NP_000029.2:p.Ile1557Asn
NM_001127510.2:c.4670T>A	NP_001120982.1:p.Ile1557Asn
NM_001127511.2:c.4616T>A	NP_001120983.2:p.Ile1539Asn
NM_001354895.1:c.4670T>A	NP_001341824.1:p.Ile1557Asn
NM_001354896.1:c.4724T>A	NP_001341825.1:p.Ile1575Asn
NM_001354897.1:c.4700T>A	NP_001341826.1:p.Ile1567Asn
NM_001354898.1:c.4595T>A	NP_001341827.1:p.Ile1532Asn
NM_001354899.1:c.4586T>A	NP_001341828.1:p.Ile1529Asn
NM_001354900.1:c.4547T>A	NP_001341829.1:p.Ile1516Asn
NM_001354901.1:c.4493T>A	NP_001341830.1:p.Ile1498Asn
NM_001354902.1:c.4397T>A	NP_001341831.1:p.Ile1466Asn
NM_001354903.1:c.4367T>A	NP_001341832.1:p.Ile1456Asn
NM_001354904.1:c.4292T>A	NP_001341833.1:p.Ile1431Asn
NM_001354905.1:c.4190T>A	NP_001341834.1:p.Ile1397Asn
NM_001354906.1:c.3821T>A	NP_001341835.1:p.Ile1274Asn
NM_000038.6:c.4670T>A MANE Select	NP_000029.2:p.Ile1557Asn
NM_001127510.3:c.4670T>A	NP_001120982.1:p.Ile1557Asn
NM_001127511.3:c.4616T>A	NP_001120983.2:p.Ile1539Asn
NM_001354895.2:c.4670T>A	NP_001341824.1:p.Ile1557Asn
NM_001354896.2:c.4724T>A	NP_001341825.1:p.Ile1575Asn
NM_001354897.2:c.4700T>A	NP_001341826.1:p.Ile1567Asn
NM_001354898.2:c.4595T>A	NP_001341827.1:p.Ile1532Asn
NM_001354899.2:c.4586T>A	NP_001341828.1:p.Ile1529Asn
NM_001354900.2:c.4547T>A	NP_001341829.1:p.Ile1516Asn
NM_001354901.2:c.4493T>A	NP_001341830.1:p.Ile1498Asn
NM_001354902.2:c.4397T>A	NP_001341831.1:p.Ile1466Asn
NM_001354903.2:c.4367T>A	NP_001341832.1:p.Ile1456Asn
NM_001354904.2:c.4292T>A	NP_001341833.1:p.Ile1431Asn
NM_001354905.2:c.4190T>A	NP_001341834.1:p.Ile1397Asn
NM_001354906.2:c.3821T>A	NP_001341835.1:p.Ile1274Asn