Canonical Allele Identifier: CA350592759

Gene: WNT10A

Linked Data

• dbSNP Id: rs778417803
• gnomAD v2: 2-219757968-C-T
• gnomAD v4: 2-218893246-C-T
• MyVariant Identifiers: chr2:g.219757968C>T (hg19) ; chr2:g.218893246C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893246C>T , CM000664.2:g.218893246C>T	GRCh38
NC_000002.11:g.219757968C>T , CM000664.1:g.219757968C>T	GRCh37
NC_000002.10:g.219466212C>T	NCBI36
NG_012179.1:g.17714C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1229C>T MANE Select	ENSP00000258411.3:p.Thr410Ile
ENST00000258411.7:c.1229C>T	ENSP00000258411.3:p.Thr410Ile
ENST00000489887.1:n.26C>T
NM_025216.2:c.1229C>T	NP_079492.2:p.Thr410Ile
XM_011511928.1:c.1178C>T	XP_011510230.1:p.Thr393Ile
XM_011511929.1:c.1133C>T	XP_011510231.1:p.Thr378Ile
XM_011511930.1:c.849C>T	XP_011510232.1:p.His283=
XM_011511929.2:c.1133C>T	XP_011510231.1:p.Thr378Ile
NM_025216.3:c.1229C>T MANE Select	NP_079492.2:p.Thr410Ile