Canonical Allele Identifier: CA416682316
Gene: WNT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.22446861T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22120368T>G , CM000663.2:g.22120368T>G GRCh38
NC_000001.10:g.22446861T>G , CM000663.1:g.22446861T>G GRCh37
NC_000001.9:g.22319448T>G NCBI36
NG_008974.1:g.27659A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290167.11:c.738A>C MANE Select ENSP00000290167.5:p.Pro246=
ENST00000290167.10:c.738A>C ENSP00000290167.5:p.Pro246=
NM_030761.4:c.738A>C NP_110388.2:p.Pro246=
XM_011541597.1:c.804A>C XP_011539899.1:p.Pro268=
XM_011541598.1:c.573A>C XP_011539900.1:p.Pro191=
XM_011541597.2:c.804A>C XP_011539899.1:p.Pro268=
XM_011541598.2:c.573A>C XP_011539900.1:p.Pro191=
NM_030761.5:c.738A>C MANE Select NP_110388.2:p.Pro246=
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