Canonical Allele Identifier: CA431416789

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218890258-C-T
• MyVariant Identifiers: chr2:g.219754980C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890258C>T , CM000664.2:g.218890258C>T	GRCh38
NC_000002.11:g.219754980C>T , CM000664.1:g.219754980C>T	GRCh37
NC_000002.10:g.219463224C>T	NCBI36
NG_012179.1:g.14726C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.651C>T MANE Select	ENSP00000258411.3:p.Asp217=
ENST00000258411.7:c.651C>T	ENSP00000258411.3:p.Asp217=
ENST00000458582.1:c.264-2516C>T
NM_025216.2:c.651C>T	NP_079492.2:p.Asp217=
XM_011511928.1:c.600C>T	XP_011510230.1:p.Asp200=
XM_011511929.1:c.555C>T	XP_011510231.1:p.Asp185=
XM_011511930.1:c.377-2516C>T	XP_011510232.1:n.377-2516C>T
XM_011511929.2:c.555C>T	XP_011510231.1:p.Asp185=
NM_025216.3:c.651C>T MANE Select	NP_079492.2:p.Asp217=