Canonical Allele Identifier: CA16031366

Gene: APC

Linked Data

• dbSNP Id: rs1561593719
• MyVariant Identifiers: chr5:g.112175874T>A (hg19) ; chr5:g.112840177T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840177T>A , CM000667.2:g.112840177T>A	GRCh38
NC_000005.9:g.112175874T>A , CM000667.1:g.112175874T>A	GRCh37
NC_000005.8:g.112203773T>A	NCBI36
NG_008481.4:g.152657T>A , LRG_130:g.152657T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4637T>A	ENSP00000473355.2:p.Val1546Asp
ENST00000505350.2:c.*4589T>A	ENSP00000481752.1:n.*4589T>A
ENST00000507379.6:c.4529T>A	ENSP00000423224.2:p.Val1510Asp
ENST00000509732.6:c.4583T>A	ENSP00000426541.2:p.Val1528Asp
ENST00000512211.7:c.4583T>A	ENSP00000423828.3:p.Val1528Asp
ENST00000257430.9:c.4583T>A MANE Select	ENSP00000257430.4:p.Val1528Asp
ENST00000257430.8:c.4583T>A	ENSP00000257430.4:p.Val1528Asp
ENST00000508376.6:c.4583T>A	ENSP00000427089.2:p.Val1528Asp
ENST00000508624.5:c.*3905T>A	ENSP00000424265.1:n.*3905T>A
ENST00000520401.1:c.230+11205T>A
NM_000038.5:c.4583T>A	NP_000029.2:p.Val1528Asp
NM_001127510.2:c.4583T>A	NP_001120982.1:p.Val1528Asp
NM_001127511.2:c.4529T>A	NP_001120983.2:p.Val1510Asp
NM_001354895.1:c.4583T>A	NP_001341824.1:p.Val1528Asp
NM_001354896.1:c.4637T>A	NP_001341825.1:p.Val1546Asp
NM_001354897.1:c.4613T>A	NP_001341826.1:p.Val1538Asp
NM_001354898.1:c.4508T>A	NP_001341827.1:p.Val1503Asp
NM_001354899.1:c.4499T>A	NP_001341828.1:p.Val1500Asp
NM_001354900.1:c.4460T>A	NP_001341829.1:p.Val1487Asp
NM_001354901.1:c.4406T>A	NP_001341830.1:p.Val1469Asp
NM_001354902.1:c.4310T>A	NP_001341831.1:p.Val1437Asp
NM_001354903.1:c.4280T>A	NP_001341832.1:p.Val1427Asp
NM_001354904.1:c.4205T>A	NP_001341833.1:p.Val1402Asp
NM_001354905.1:c.4103T>A	NP_001341834.1:p.Val1368Asp
NM_001354906.1:c.3734T>A	NP_001341835.1:p.Val1245Asp
NM_000038.6:c.4583T>A MANE Select	NP_000029.2:p.Val1528Asp
NM_001127510.3:c.4583T>A	NP_001120982.1:p.Val1528Asp
NM_001127511.3:c.4529T>A	NP_001120983.2:p.Val1510Asp
NM_001354895.2:c.4583T>A	NP_001341824.1:p.Val1528Asp
NM_001354896.2:c.4637T>A	NP_001341825.1:p.Val1546Asp
NM_001354897.2:c.4613T>A	NP_001341826.1:p.Val1538Asp
NM_001354898.2:c.4508T>A	NP_001341827.1:p.Val1503Asp
NM_001354899.2:c.4499T>A	NP_001341828.1:p.Val1500Asp
NM_001354900.2:c.4460T>A	NP_001341829.1:p.Val1487Asp
NM_001354901.2:c.4406T>A	NP_001341830.1:p.Val1469Asp
NM_001354902.2:c.4310T>A	NP_001341831.1:p.Val1437Asp
NM_001354903.2:c.4280T>A	NP_001341832.1:p.Val1427Asp
NM_001354904.2:c.4205T>A	NP_001341833.1:p.Val1402Asp
NM_001354905.2:c.4103T>A	NP_001341834.1:p.Val1368Asp
NM_001354906.2:c.3734T>A	NP_001341835.1:p.Val1245Asp