Canonical Allele Identifier: CA350592243

Gene: WNT10A

Linked Data

• dbSNP Id: rs1412307290
• gnomAD v2: 2-219757914-G-T
• gnomAD v4: 2-218893192-G-T
• MyVariant Identifiers: chr2:g.219757914G>T (hg19) ; chr2:g.218893192G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893192G>T , CM000664.2:g.218893192G>T	GRCh38
NC_000002.11:g.219757914G>T , CM000664.1:g.219757914G>T	GRCh37
NC_000002.10:g.219466158G>T	NCBI36
NG_012179.1:g.17660G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1175G>T MANE Select	ENSP00000258411.3:p.Cys392Phe
ENST00000258411.7:c.1175G>T	ENSP00000258411.3:p.Cys392Phe
NM_025216.2:c.1175G>T	NP_079492.2:p.Cys392Phe
XM_011511928.1:c.1124G>T	XP_011510230.1:p.Cys375Phe
XM_011511929.1:c.1079G>T	XP_011510231.1:p.Cys360Phe
XM_011511930.1:c.795G>T	XP_011510232.1:p.Leu265=
XM_011511929.2:c.1079G>T	XP_011510231.1:p.Cys360Phe
NM_025216.3:c.1175G>T MANE Select	NP_079492.2:p.Cys392Phe