Canonical Allele Identifier: CA2577276400

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893177_218893181del , CM000664.2:g.218893177_218893181del	GRCh38
NC_000002.11:g.219757899_219757903del , CM000664.1:g.219757899_219757903del	GRCh37
NC_000002.10:g.219466143_219466147del	NCBI36
NG_012179.1:g.17645_17649del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1160_1164del MANE Select	ENSP00000258411.3:p.Thr387LysfsTer?
ENST00000258411.7:c.1160_1164del	ENSP00000258411.3:p.Thr387LysfsTer?
NM_025216.2:c.1160_1164del	NP_079492.2:p.Thr387LysfsTer?
XM_011511928.1:c.1109_1113del	XP_011510230.1:p.Thr370LysfsTer?
XM_011511929.1:c.1064_1068del	XP_011510231.1:p.Thr355LysfsTer?
XM_011511930.1:c.780_784del	XP_011510232.1:p.Asp260GlufsTer?
XM_011511929.2:c.1064_1068del	XP_011510231.1:p.Thr355LysfsTer?
NM_025216.3:c.1160_1164del MANE Select	NP_079492.2:p.Thr387LysfsTer?