Canonical Allele Identifier: CA16024891
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828869T>A , CM000667.2:g.112828869T>A GRCh38
NC_000005.9:g.112164566T>A , CM000667.1:g.112164566T>A GRCh37
NC_000005.8:g.112192465T>A NCBI36
NG_008481.4:g.141349T>A , LRG_130:g.141349T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257430.9:c.1640T>A MANE Select ENSP00000257430.4:p.Val547Asp
ENST00000257430.8:c.1640T>A ENSP00000257430.4:p.Val547Asp
ENST00000502371.2:n.97-6082T>A
ENST00000504915.2:n.329T>A ENSP00000473355.1:p.Val110Asp
ENST00000505084.1:n.127T>A
ENST00000507379.5:c.1586T>A ENSP00000423224.1:p.Val529Asp
ENST00000508376.6:c.1640T>A ENSP00000427089.2:p.Val547Asp
ENST00000508624.5:c.*962T>A ENSP00000424265.1:n.*962T>A
ENST00000512211.6:c.1640T>A ENSP00000423828.2:p.Val547Asp
ENST00000520401.1:n.127T>A
NM_000038.5:c.1640T>A NP_000029.2:p.Val547Asp
NM_001127510.2:c.1640T>A NP_001120982.1:p.Val547Asp
NM_001127511.2:c.1586T>A NP_001120983.2:p.Val529Asp
NM_001354895.1:c.1640T>A NP_001341824.1:p.Val547Asp
NM_001354896.1:c.1694T>A NP_001341825.1:p.Val565Asp
NM_001354897.1:c.1670T>A NP_001341826.1:p.Val557Asp
NM_001354898.1:c.1565T>A NP_001341827.1:p.Val522Asp
NM_001354899.1:c.1556T>A NP_001341828.1:p.Val519Asp
NM_001354900.1:c.1517T>A NP_001341829.1:p.Val506Asp
NM_001354901.1:c.1463T>A NP_001341830.1:p.Val488Asp
NM_001354902.1:c.1367T>A NP_001341831.1:p.Val456Asp
NM_001354903.1:c.1337T>A NP_001341832.1:p.Val446Asp
NM_001354904.1:c.1262T>A NP_001341833.1:p.Val421Asp
NM_001354905.1:c.1160T>A NP_001341834.1:p.Val387Asp
NM_001354906.1:c.791T>A NP_001341835.1:p.Val264Asp
NM_000038.6:c.1640T>A MANE Select NP_000029.2:p.Val547Asp
NM_001127510.3:c.1640T>A NP_001120982.1:p.Val547Asp
NM_001127511.3:c.1586T>A NP_001120983.2:p.Val529Asp
NM_001354895.2:c.1640T>A NP_001341824.1:p.Val547Asp
NM_001354896.2:c.1694T>A NP_001341825.1:p.Val565Asp
NM_001354897.2:c.1670T>A NP_001341826.1:p.Val557Asp
NM_001354898.2:c.1565T>A NP_001341827.1:p.Val522Asp
NM_001354899.2:c.1556T>A NP_001341828.1:p.Val519Asp
NM_001354900.2:c.1517T>A NP_001341829.1:p.Val506Asp
NM_001354901.2:c.1463T>A NP_001341830.1:p.Val488Asp
NM_001354902.2:c.1367T>A NP_001341831.1:p.Val456Asp
NM_001354903.2:c.1337T>A NP_001341832.1:p.Val446Asp
NM_001354904.2:c.1262T>A NP_001341833.1:p.Val421Asp
NM_001354905.2:c.1160T>A NP_001341834.1:p.Val387Asp
NM_001354906.2:c.791T>A NP_001341835.1:p.Val264Asp