Canonical Allele Identifier: CA350618238

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746930T>C (hg19) ; chr2:g.218882208T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882208T>C , CM000664.2:g.218882208T>C	GRCh38
NC_000002.11:g.219746930T>C , CM000664.1:g.219746930T>C	GRCh37
NC_000002.10:g.219455174T>C	NCBI36
NG_012179.1:g.6676T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.161T>C MANE Select	ENSP00000258411.3:p.Val54Ala
ENST00000258411.7:c.161T>C	ENSP00000258411.3:p.Val54Ala
ENST00000458582.1:c.48T>C
NM_025216.2:c.161T>C	NP_079492.2:p.Val54Ala
XM_011511928.1:c.110T>C	XP_011510230.1:p.Val37Ala
XM_011511929.1:c.65T>C	XP_011510231.1:p.Val22Ala
XM_011511930.1:c.161T>C	XP_011510232.1:p.Val54Ala
XM_011511929.2:c.65T>C	XP_011510231.1:p.Val22Ala
NM_025216.3:c.161T>C MANE Select	NP_079492.2:p.Val54Ala