Canonical Allele Identifier: CA350592764

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893248-G-C
• MyVariant Identifiers: chr2:g.219757970G>C (hg19) ; chr2:g.218893248G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893248G>C , CM000664.2:g.218893248G>C	GRCh38
NC_000002.11:g.219757970G>C , CM000664.1:g.219757970G>C	GRCh37
NC_000002.10:g.219466214G>C	NCBI36
NG_012179.1:g.17716G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1231G>C MANE Select	ENSP00000258411.3:p.Glu411Gln
ENST00000258411.7:c.1231G>C	ENSP00000258411.3:p.Glu411Gln
ENST00000489887.1:n.28G>C
NM_025216.2:c.1231G>C	NP_079492.2:p.Glu411Gln
XM_011511928.1:c.1180G>C	XP_011510230.1:p.Glu394Gln
XM_011511929.1:c.1135G>C	XP_011510231.1:p.Glu379Gln
XM_011511930.1:c.851G>C	XP_011510232.1:p.Arg284Pro
XM_011511929.2:c.1135G>C	XP_011510231.1:p.Glu379Gln
NM_025216.3:c.1231G>C MANE Select	NP_079492.2:p.Glu411Gln