Canonical Allele Identifier: CA16024893
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 643367

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000257430.9:c.1640T>G MANE Select ENSP00000257430.4:p.Val547Gly
ENST00000257430.8:c.1640T>G ENSP00000257430.4:p.Val547Gly
ENST00000502371.2:n.97-6082T>G
ENST00000504915.2:n.329T>G ENSP00000473355.1:p.Val110Gly
ENST00000505084.1:n.127T>G
ENST00000507379.5:c.1586T>G ENSP00000423224.1:p.Val529Gly
ENST00000508376.6:c.1640T>G ENSP00000427089.2:p.Val547Gly
ENST00000508624.5:c.*962T>G ENSP00000424265.1:n.*962T>G
ENST00000512211.6:c.1640T>G ENSP00000423828.2:p.Val547Gly
ENST00000520401.1:n.127T>G
NM_000038.5:c.1640T>G NP_000029.2:p.Val547Gly
NM_001127510.2:c.1640T>G NP_001120982.1:p.Val547Gly
NM_001127511.2:c.1586T>G NP_001120983.2:p.Val529Gly
NM_001354895.1:c.1640T>G NP_001341824.1:p.Val547Gly
NM_001354896.1:c.1694T>G NP_001341825.1:p.Val565Gly
NM_001354897.1:c.1670T>G NP_001341826.1:p.Val557Gly
NM_001354898.1:c.1565T>G NP_001341827.1:p.Val522Gly
NM_001354899.1:c.1556T>G NP_001341828.1:p.Val519Gly
NM_001354900.1:c.1517T>G NP_001341829.1:p.Val506Gly
NM_001354901.1:c.1463T>G NP_001341830.1:p.Val488Gly
NM_001354902.1:c.1367T>G NP_001341831.1:p.Val456Gly
NM_001354903.1:c.1337T>G NP_001341832.1:p.Val446Gly
NM_001354904.1:c.1262T>G NP_001341833.1:p.Val421Gly
NM_001354905.1:c.1160T>G NP_001341834.1:p.Val387Gly
NM_001354906.1:c.791T>G NP_001341835.1:p.Val264Gly
NM_000038.6:c.1640T>G MANE Select NP_000029.2:p.Val547Gly
NM_001127510.3:c.1640T>G NP_001120982.1:p.Val547Gly
NM_001127511.3:c.1586T>G NP_001120983.2:p.Val529Gly
NM_001354895.2:c.1640T>G NP_001341824.1:p.Val547Gly
NM_001354896.2:c.1694T>G NP_001341825.1:p.Val565Gly
NM_001354897.2:c.1670T>G NP_001341826.1:p.Val557Gly
NM_001354898.2:c.1565T>G NP_001341827.1:p.Val522Gly
NM_001354899.2:c.1556T>G NP_001341828.1:p.Val519Gly
NM_001354900.2:c.1517T>G NP_001341829.1:p.Val506Gly
NM_001354901.2:c.1463T>G NP_001341830.1:p.Val488Gly
NM_001354902.2:c.1367T>G NP_001341831.1:p.Val456Gly
NM_001354903.2:c.1337T>G NP_001341832.1:p.Val446Gly
NM_001354904.2:c.1262T>G NP_001341833.1:p.Val421Gly
NM_001354905.2:c.1160T>G NP_001341834.1:p.Val387Gly
NM_001354906.2:c.791T>G NP_001341835.1:p.Val264Gly