Canonical Allele Identifier: CA445757378
Gene: APC HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.112164567T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828870T>G , CM000667.2:g.112828870T>G GRCh38
NC_000005.9:g.112164567T>G , CM000667.1:g.112164567T>G GRCh37
NC_000005.8:g.112192466T>G NCBI36
NG_008481.4:g.141350T>G , LRG_130:g.141350T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1409-6081T>G ENSP00000484935.2:n.1409-6081T>G
ENST00000504915.3:c.1695T>G ENSP00000473355.2:p.Val565=
ENST00000505084.2:n.1697T>G
ENST00000505350.2:c.*1647T>G ENSP00000481752.1:n.*1647T>G
ENST00000507379.6:c.1587T>G ENSP00000423224.2:p.Val529=
ENST00000509732.6:c.1641T>G ENSP00000426541.2:p.Val547=
ENST00000512211.7:c.1641T>G ENSP00000423828.3:p.Val547=
ENST00000257430.9:c.1641T>G MANE Select ENSP00000257430.4:p.Val547=
ENST00000257430.8:c.1641T>G ENSP00000257430.4:p.Val547=
ENST00000502371.2:c.97-6081T>G
ENST00000504915.2:c.330T>G ENSP00000473355.1:p.Val110=
ENST00000505084.1:n.128T>G
ENST00000507379.5:c.1587T>G ENSP00000423224.1:p.Val529=
ENST00000508376.6:c.1641T>G ENSP00000427089.2:p.Val547=
ENST00000508624.5:c.*963T>G ENSP00000424265.1:n.*963T>G
ENST00000512211.6:c.1641T>G ENSP00000423828.2:p.Val547=
ENST00000520401.1:c.128T>G
NM_000038.5:c.1641T>G NP_000029.2:p.Val547=
NM_001127510.2:c.1641T>G NP_001120982.1:p.Val547=
NM_001127511.2:c.1587T>G NP_001120983.2:p.Val529=
NM_001354895.1:c.1641T>G NP_001341824.1:p.Val547=
NM_001354896.1:c.1695T>G NP_001341825.1:p.Val565=
NM_001354897.1:c.1671T>G NP_001341826.1:p.Val557=
NM_001354898.1:c.1566T>G NP_001341827.1:p.Val522=
NM_001354899.1:c.1557T>G NP_001341828.1:p.Val519=
NM_001354900.1:c.1518T>G NP_001341829.1:p.Val506=
NM_001354901.1:c.1464T>G NP_001341830.1:p.Val488=
NM_001354902.1:c.1368T>G NP_001341831.1:p.Val456=
NM_001354903.1:c.1338T>G NP_001341832.1:p.Val446=
NM_001354904.1:c.1263T>G NP_001341833.1:p.Val421=
NM_001354905.1:c.1161T>G NP_001341834.1:p.Val387=
NM_001354906.1:c.792T>G NP_001341835.1:p.Val264=
NM_000038.6:c.1641T>G MANE Select NP_000029.2:p.Val547=
NM_001127510.3:c.1641T>G NP_001120982.1:p.Val547=
NM_001127511.3:c.1587T>G NP_001120983.2:p.Val529=
NM_001354895.2:c.1641T>G NP_001341824.1:p.Val547=
NM_001354896.2:c.1695T>G NP_001341825.1:p.Val565=
NM_001354897.2:c.1671T>G NP_001341826.1:p.Val557=
NM_001354898.2:c.1566T>G NP_001341827.1:p.Val522=
NM_001354899.2:c.1557T>G NP_001341828.1:p.Val519=
NM_001354900.2:c.1518T>G NP_001341829.1:p.Val506=
NM_001354901.2:c.1464T>G NP_001341830.1:p.Val488=
NM_001354902.2:c.1368T>G NP_001341831.1:p.Val456=
NM_001354903.2:c.1338T>G NP_001341832.1:p.Val446=
NM_001354904.2:c.1263T>G NP_001341833.1:p.Val421=
NM_001354905.2:c.1161T>G NP_001341834.1:p.Val387=
NM_001354906.2:c.792T>G NP_001341835.1:p.Val264=