Canonical Allele Identifier: CA2838198950

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129587C>T , CM000663.2:g.22129587C>T	GRCh38
NC_000001.10:g.22456080C>T , CM000663.1:g.22456080C>T	GRCh37
NC_000001.9:g.22328667C>T	NCBI36
NG_008974.1:g.18440G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.313+29G>A MANE Select	ENSP00000290167.5:n.313+29G>A
ENST00000290167.10:c.313+29G>A	ENSP00000290167.5:n.313+29G>A
ENST00000415567.1:c.236+29G>A
ENST00000441048.1:c.148+29G>A	ENSP00000388925.1:n.148+29G>A
NM_030761.4:c.313+29G>A	NP_110388.2:n.313+29G>A
XM_011541597.1:c.379+29G>A	XP_011539899.1:n.379+29G>A
XM_011541598.1:c.148+29G>A	XP_011539900.1:n.148+29G>A
XM_011541599.1:c.379+29G>A	XP_011539901.1:n.379+29G>A
XM_011541597.2:c.379+29G>A	XP_011539899.1:n.379+29G>A
XM_011541598.2:c.148+29G>A	XP_011539900.1:n.148+29G>A
NM_030761.5:c.313+29G>A MANE Select	NP_110388.2:n.313+29G>A