Canonical Allele Identifier: CA1158260766

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129582G= , CM000663.2:g.22129582G=	GRCh38
NC_000001.10:g.22456075G= , CM000663.1:g.22456075G=	GRCh37
NC_000001.9:g.22328662G=	NCBI36
NG_008974.1:g.18445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.313+34C= MANE Select	ENSP00000290167.5:n.313+34C=
ENST00000290167.10:c.313+34C=	ENSP00000290167.5:n.313+34C=
ENST00000415567.1:c.236+34C=
ENST00000441048.1:c.148+34C=	ENSP00000388925.1:n.148+34C=
NM_030761.4:c.313+34C=	NP_110388.2:n.313+34C=
XM_011541597.1:c.379+34C=	XP_011539899.1:n.379+34C=
XM_011541598.1:c.148+34C=	XP_011539900.1:n.148+34C=
XM_011541599.1:c.379+34C=	XP_011539901.1:n.379+34C=
XM_011541597.2:c.379+34C=	XP_011539899.1:n.379+34C=
XM_011541598.2:c.148+34C=	XP_011539900.1:n.148+34C=
NM_030761.5:c.313+34C= MANE Select	NP_110388.2:n.313+34C=