Canonical Allele Identifier: CA445757382
Gene: APC HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.112164571A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828874A>C , CM000667.2:g.112828874A>C GRCh38
NC_000005.9:g.112164571A>C , CM000667.1:g.112164571A>C GRCh37
NC_000005.8:g.112192470A>C NCBI36
NG_008481.4:g.141354A>C , LRG_130:g.141354A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000257430.9:c.1645A>C MANE Select ENSP00000257430.4:p.Arg549=
ENST00000257430.8:c.1645A>C ENSP00000257430.4:p.Arg549=
ENST00000502371.2:n.97-6077A>C
ENST00000504915.2:n.334A>C ENSP00000473355.1:p.Arg112=
ENST00000505084.1:n.132A>C
ENST00000507379.5:c.1591A>C ENSP00000423224.1:p.Arg531=
ENST00000508376.6:c.1645A>C ENSP00000427089.2:p.Arg549=
ENST00000508624.5:c.*967A>C ENSP00000424265.1:n.*967A>C
ENST00000512211.6:c.1645A>C ENSP00000423828.2:p.Arg549=
ENST00000520401.1:n.132A>C
NM_000038.5:c.1645A>C NP_000029.2:p.Arg549=
NM_001127510.2:c.1645A>C NP_001120982.1:p.Arg549=
NM_001127511.2:c.1591A>C NP_001120983.2:p.Arg531=
NM_001354895.1:c.1645A>C NP_001341824.1:p.Arg549=
NM_001354896.1:c.1699A>C NP_001341825.1:p.Arg567=
NM_001354897.1:c.1675A>C NP_001341826.1:p.Arg559=
NM_001354898.1:c.1570A>C NP_001341827.1:p.Arg524=
NM_001354899.1:c.1561A>C NP_001341828.1:p.Arg521=
NM_001354900.1:c.1522A>C NP_001341829.1:p.Arg508=
NM_001354901.1:c.1468A>C NP_001341830.1:p.Arg490=
NM_001354902.1:c.1372A>C NP_001341831.1:p.Arg458=
NM_001354903.1:c.1342A>C NP_001341832.1:p.Arg448=
NM_001354904.1:c.1267A>C NP_001341833.1:p.Arg423=
NM_001354905.1:c.1165A>C NP_001341834.1:p.Arg389=
NM_001354906.1:c.796A>C NP_001341835.1:p.Arg266=
NM_000038.6:c.1645A>C MANE Select NP_000029.2:p.Arg549=
NM_001127510.3:c.1645A>C NP_001120982.1:p.Arg549=
NM_001127511.3:c.1591A>C NP_001120983.2:p.Arg531=
NM_001354895.2:c.1645A>C NP_001341824.1:p.Arg549=
NM_001354896.2:c.1699A>C NP_001341825.1:p.Arg567=
NM_001354897.2:c.1675A>C NP_001341826.1:p.Arg559=
NM_001354898.2:c.1570A>C NP_001341827.1:p.Arg524=
NM_001354899.2:c.1561A>C NP_001341828.1:p.Arg521=
NM_001354900.2:c.1522A>C NP_001341829.1:p.Arg508=
NM_001354901.2:c.1468A>C NP_001341830.1:p.Arg490=
NM_001354902.2:c.1372A>C NP_001341831.1:p.Arg458=
NM_001354903.2:c.1342A>C NP_001341832.1:p.Arg448=
NM_001354904.2:c.1267A>C NP_001341833.1:p.Arg423=
NM_001354905.2:c.1165A>C NP_001341834.1:p.Arg389=
NM_001354906.2:c.796A>C NP_001341835.1:p.Arg266=