Canonical Allele Identifier: CA431234859

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893247-C-T
• MyVariant Identifiers: chr2:g.219757969C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893247C>T , CM000664.2:g.218893247C>T	GRCh38
NC_000002.11:g.219757969C>T , CM000664.1:g.219757969C>T	GRCh37
NC_000002.10:g.219466213C>T	NCBI36
NG_012179.1:g.17715C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1230C>T MANE Select	ENSP00000258411.3:p.Thr410=
ENST00000258411.7:c.1230C>T	ENSP00000258411.3:p.Thr410=
ENST00000489887.1:n.27C>T
NM_025216.2:c.1230C>T	NP_079492.2:p.Thr410=
XM_011511928.1:c.1179C>T	XP_011510230.1:p.Thr393=
XM_011511929.1:c.1134C>T	XP_011510231.1:p.Thr378=
XM_011511930.1:c.850C>T	XP_011510232.1:p.Arg284Ter
XM_011511929.2:c.1134C>T	XP_011510231.1:p.Thr378=
NM_025216.3:c.1230C>T MANE Select	NP_079492.2:p.Thr410=