Canonical Allele Identifier: CA16032261

Gene: APC

Linked Data

• ClinVar Variation Id: 802145
• ClinVar RCV Id: RCV000987576
• dbSNP Id: rs1176817504
• MyVariant Identifiers: chr5:g.112176285C>A (hg19) ; chr5:g.112840588C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840588C>A , CM000667.2:g.112840588C>A	GRCh38
NC_000005.9:g.112176285C>A , CM000667.1:g.112176285C>A	GRCh37
NC_000005.8:g.112204184C>A	NCBI36
NG_008481.4:g.153068C>A , LRG_130:g.153068C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5048C>A	ENSP00000473355.2:p.Pro1683His
ENST00000505350.2:c.*5000C>A	ENSP00000481752.1:n.*5000C>A
ENST00000507379.6:c.4940C>A	ENSP00000423224.2:p.Pro1647His
ENST00000509732.6:c.4994C>A	ENSP00000426541.2:p.Pro1665His
ENST00000512211.7:c.4994C>A	ENSP00000423828.3:p.Pro1665His
ENST00000257430.9:c.4994C>A MANE Select	ENSP00000257430.4:p.Pro1665His
ENST00000257430.8:c.4994C>A	ENSP00000257430.4:p.Pro1665His
ENST00000508376.6:c.4994C>A	ENSP00000427089.2:p.Pro1665His
ENST00000508624.5:c.*4316C>A	ENSP00000424265.1:n.*4316C>A
ENST00000520401.1:c.230+11616C>A
NM_000038.5:c.4994C>A	NP_000029.2:p.Pro1665His
NM_001127510.2:c.4994C>A	NP_001120982.1:p.Pro1665His
NM_001127511.2:c.4940C>A	NP_001120983.2:p.Pro1647His
NM_001354895.1:c.4994C>A	NP_001341824.1:p.Pro1665His
NM_001354896.1:c.5048C>A	NP_001341825.1:p.Pro1683His
NM_001354897.1:c.5024C>A	NP_001341826.1:p.Pro1675His
NM_001354898.1:c.4919C>A	NP_001341827.1:p.Pro1640His
NM_001354899.1:c.4910C>A	NP_001341828.1:p.Pro1637His
NM_001354900.1:c.4871C>A	NP_001341829.1:p.Pro1624His
NM_001354901.1:c.4817C>A	NP_001341830.1:p.Pro1606His
NM_001354902.1:c.4721C>A	NP_001341831.1:p.Pro1574His
NM_001354903.1:c.4691C>A	NP_001341832.1:p.Pro1564His
NM_001354904.1:c.4616C>A	NP_001341833.1:p.Pro1539His
NM_001354905.1:c.4514C>A	NP_001341834.1:p.Pro1505His
NM_001354906.1:c.4145C>A	NP_001341835.1:p.Pro1382His
NM_000038.6:c.4994C>A MANE Select	NP_000029.2:p.Pro1665His
NM_001127510.3:c.4994C>A	NP_001120982.1:p.Pro1665His
NM_001127511.3:c.4940C>A	NP_001120983.2:p.Pro1647His
NM_001354895.2:c.4994C>A	NP_001341824.1:p.Pro1665His
NM_001354896.2:c.5048C>A	NP_001341825.1:p.Pro1683His
NM_001354897.2:c.5024C>A	NP_001341826.1:p.Pro1675His
NM_001354898.2:c.4919C>A	NP_001341827.1:p.Pro1640His
NM_001354899.2:c.4910C>A	NP_001341828.1:p.Pro1637His
NM_001354900.2:c.4871C>A	NP_001341829.1:p.Pro1624His
NM_001354901.2:c.4817C>A	NP_001341830.1:p.Pro1606His
NM_001354902.2:c.4721C>A	NP_001341831.1:p.Pro1574His
NM_001354903.2:c.4691C>A	NP_001341832.1:p.Pro1564His
NM_001354904.2:c.4616C>A	NP_001341833.1:p.Pro1539His
NM_001354905.2:c.4514C>A	NP_001341834.1:p.Pro1505His
NM_001354906.2:c.4145C>A	NP_001341835.1:p.Pro1382His