Canonical Allele Identifier: CA350592346

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893203-T-C
• MyVariant Identifiers: chr2:g.219757925T>C (hg19) ; chr2:g.218893203T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893203T>C , CM000664.2:g.218893203T>C	GRCh38
NC_000002.11:g.219757925T>C , CM000664.1:g.219757925T>C	GRCh37
NC_000002.10:g.219466169T>C	NCBI36
NG_012179.1:g.17671T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1186T>C MANE Select	ENSP00000258411.3:p.Phe396Leu
ENST00000258411.7:c.1186T>C	ENSP00000258411.3:p.Phe396Leu
NM_025216.2:c.1186T>C	NP_079492.2:p.Phe396Leu
XM_011511928.1:c.1135T>C	XP_011510230.1:p.Phe379Leu
XM_011511929.1:c.1090T>C	XP_011510231.1:p.Phe364Leu
XM_011511930.1:c.806T>C	XP_011510232.1:p.Leu269Pro
XM_011511929.2:c.1090T>C	XP_011510231.1:p.Phe364Leu
NM_025216.3:c.1186T>C MANE Select	NP_079492.2:p.Phe396Leu