Canonical Allele Identifier: CA350592618

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893228-G-T
• MyVariant Identifiers: chr2:g.219757950G>T (hg19) ; chr2:g.218893228G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893228G>T , CM000664.2:g.218893228G>T	GRCh38
NC_000002.11:g.219757950G>T , CM000664.1:g.219757950G>T	GRCh37
NC_000002.10:g.219466194G>T	NCBI36
NG_012179.1:g.17696G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1211G>T MANE Select	ENSP00000258411.3:p.Cys404Phe
ENST00000258411.7:c.1211G>T	ENSP00000258411.3:p.Cys404Phe
ENST00000489887.1:n.8G>T
NM_025216.2:c.1211G>T	NP_079492.2:p.Cys404Phe
XM_011511928.1:c.1160G>T	XP_011510230.1:p.Cys387Phe
XM_011511929.1:c.1115G>T	XP_011510231.1:p.Cys372Phe
XM_011511930.1:c.831G>T	XP_011510232.1:p.Leu277=
XM_011511929.2:c.1115G>T	XP_011510231.1:p.Cys372Phe
NM_025216.3:c.1211G>T MANE Select	NP_079492.2:p.Cys404Phe