Canonical Allele Identifier: CA1328965719

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893291_218893292delinsGC , CM000664.2:g.218893291_218893292delinsGC	GRCh38
NC_000002.11:g.219758013_219758014delinsGC , CM000664.1:g.219758013_219758014delinsGC	GRCh37
NC_000002.10:g.219466257_219466258delinsGC	NCBI36
NG_012179.1:g.17759_17760delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*20_*21delinsGC MANE Select	ENSP00000258411.3:n.*20_*21delinsGC
ENST00000258411.7:c.*20_*21delinsGC	ENSP00000258411.3:n.*20_*21delinsGC
ENST00000489887.1:n.47+24_47+25delinsGC
NM_025216.2:c.*20_*21delinsGC	NP_079492.2:n.*20_*21delinsGC
XM_011511928.1:c.*20_*21delinsGC	XP_011510230.1:n.*20_*21delinsGC
XM_011511929.1:c.*20_*21delinsGC	XP_011510231.1:n.*20_*21delinsGC
XM_011511930.1:c.894_895delinsGC	XP_011510232.1:p.Gly298=
XM_011511929.2:c.*20_*21delinsGC	XP_011510231.1:n.*20_*21delinsGC
NM_025216.3:c.*20_*21delinsGC MANE Select	NP_079492.2:n.*20_*21delinsGC