Canonical Allele Identifier: CA1328961545

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882241_218882242delinsCA , CM000664.2:g.218882241_218882242delinsCA	GRCh38
NC_000002.11:g.219746963_219746964delinsCA , CM000664.1:g.219746963_219746964delinsCA	GRCh37
NC_000002.10:g.219455207_219455208delinsCA	NCBI36
NG_012179.1:g.6709_6710delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.194_195delinsCA MANE Select	ENSP00000258411.3:p.Pro65=
ENST00000258411.7:c.194_195delinsCA	ENSP00000258411.3:p.Pro65=
ENST00000458582.1:c.81_82delinsCA
NM_025216.2:c.194_195delinsCA	NP_079492.2:p.Pro65=
XM_011511928.1:c.143_144delinsCA	XP_011510230.1:p.Pro48=
XM_011511929.1:c.98_99delinsCA	XP_011510231.1:p.Pro33=
XM_011511930.1:c.194_195delinsCA	XP_011510232.1:p.Pro65=
XM_011511929.2:c.98_99delinsCA	XP_011510231.1:p.Pro33=
NM_025216.3:c.194_195delinsCA MANE Select	NP_079492.2:p.Pro65=