Canonical Allele Identifier: CA1573472278
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840484T= , CM000667.2:g.112840484T= GRCh38
NC_000005.9:g.112176181T= , CM000667.1:g.112176181T= GRCh37
NC_000005.8:g.112204080T= NCBI36
NG_008481.4:g.152964T= , LRG_130:g.152964T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.4944T= ENSP00000473355.2:p.Val1648=
ENST00000505350.2:c.*4896T= ENSP00000481752.1:n.*4896T=
ENST00000507379.6:c.4836T= ENSP00000423224.2:p.Val1612=
ENST00000509732.6:c.4890T= ENSP00000426541.2:p.Val1630=
ENST00000512211.7:c.4890T= ENSP00000423828.3:p.Val1630=
ENST00000257430.9:c.4890T= MANE Select ENSP00000257430.4:p.Val1630=
ENST00000257430.8:c.4890T= ENSP00000257430.4:p.Val1630=
ENST00000508376.6:c.4890T= ENSP00000427089.2:p.Val1630=
ENST00000508624.5:c.*4212T= ENSP00000424265.1:n.*4212T=
ENST00000520401.1:c.230+11512T=
NM_000038.5:c.4890T= NP_000029.2:p.Val1630=
NM_001127510.2:c.4890T= NP_001120982.1:p.Val1630=
NM_001127511.2:c.4836T= NP_001120983.2:p.Val1612=
NM_001354895.1:c.4890T= NP_001341824.1:p.Val1630=
NM_001354896.1:c.4944T= NP_001341825.1:p.Val1648=
NM_001354897.1:c.4920T= NP_001341826.1:p.Val1640=
NM_001354898.1:c.4815T= NP_001341827.1:p.Val1605=
NM_001354899.1:c.4806T= NP_001341828.1:p.Val1602=
NM_001354900.1:c.4767T= NP_001341829.1:p.Val1589=
NM_001354901.1:c.4713T= NP_001341830.1:p.Val1571=
NM_001354902.1:c.4617T= NP_001341831.1:p.Val1539=
NM_001354903.1:c.4587T= NP_001341832.1:p.Val1529=
NM_001354904.1:c.4512T= NP_001341833.1:p.Val1504=
NM_001354905.1:c.4410T= NP_001341834.1:p.Val1470=
NM_001354906.1:c.4041T= NP_001341835.1:p.Val1347=
NM_000038.6:c.4890T= MANE Select NP_000029.2:p.Val1630=
NM_001127510.3:c.4890T= NP_001120982.1:p.Val1630=
NM_001127511.3:c.4836T= NP_001120983.2:p.Val1612=
NM_001354895.2:c.4890T= NP_001341824.1:p.Val1630=
NM_001354896.2:c.4944T= NP_001341825.1:p.Val1648=
NM_001354897.2:c.4920T= NP_001341826.1:p.Val1640=
NM_001354898.2:c.4815T= NP_001341827.1:p.Val1605=
NM_001354899.2:c.4806T= NP_001341828.1:p.Val1602=
NM_001354900.2:c.4767T= NP_001341829.1:p.Val1589=
NM_001354901.2:c.4713T= NP_001341830.1:p.Val1571=
NM_001354902.2:c.4617T= NP_001341831.1:p.Val1539=
NM_001354903.2:c.4587T= NP_001341832.1:p.Val1529=
NM_001354904.2:c.4512T= NP_001341833.1:p.Val1504=
NM_001354905.2:c.4410T= NP_001341834.1:p.Val1470=
NM_001354906.2:c.4041T= NP_001341835.1:p.Val1347=