Canonical Allele Identifier: CA1158260776

Gene: WNT4

Linked Data

• dbSNP Id: rs369787887

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129602C>A , CM000663.2:g.22129602C>A	GRCh38
NC_000001.10:g.22456095C>A , CM000663.1:g.22456095C>A	GRCh37
NC_000001.9:g.22328682C>A	NCBI36
NG_008974.1:g.18425G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.313+14G>T MANE Select	ENSP00000290167.5:n.313+14G>T
ENST00000290167.10:c.313+14G>T	ENSP00000290167.5:n.313+14G>T
ENST00000415567.1:c.236+14G>T
ENST00000441048.1:c.148+14G>T	ENSP00000388925.1:n.148+14G>T
NM_030761.4:c.313+14G>T	NP_110388.2:n.313+14G>T
XM_011541597.1:c.379+14G>T	XP_011539899.1:n.379+14G>T
XM_011541598.1:c.148+14G>T	XP_011539900.1:n.148+14G>T
XM_011541599.1:c.379+14G>T	XP_011539901.1:n.379+14G>T
XM_011541597.2:c.379+14G>T	XP_011539899.1:n.379+14G>T
XM_011541598.2:c.148+14G>T	XP_011539900.1:n.148+14G>T
NM_030761.5:c.313+14G>T MANE Select	NP_110388.2:n.313+14G>T