Canonical Allele Identifier: CA65916870

Gene: WNT10A

Linked Data

• dbSNP Id: rs373991357
• gnomAD v2: 2-219754981-A-C
• gnomAD v4: 2-218890259-A-C
• MyVariant Identifiers: chr2:g.219754981A>C (hg19) ; chr2:g.218890259A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890259A>C , CM000664.2:g.218890259A>C	GRCh38
NC_000002.11:g.219754981A>C , CM000664.1:g.219754981A>C	GRCh37
NC_000002.10:g.219463225A>C	NCBI36
NG_012179.1:g.14727A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.652A>C MANE Select	ENSP00000258411.3:p.Met218Leu
ENST00000258411.7:c.652A>C	ENSP00000258411.3:p.Met218Leu
ENST00000458582.1:c.264-2515A>C
NM_025216.2:c.652A>C	NP_079492.2:p.Met218Leu
XM_011511928.1:c.601A>C	XP_011510230.1:p.Met201Leu
XM_011511929.1:c.556A>C	XP_011510231.1:p.Met186Leu
XM_011511930.1:c.377-2515A>C	XP_011510232.1:n.377-2515A>C
XM_011511929.2:c.556A>C	XP_011510231.1:p.Met186Leu
NM_025216.3:c.652A>C MANE Select	NP_079492.2:p.Met218Leu