Canonical Allele Identifier: CA1328961301

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881700_218881704delinsTTGTG , CM000664.2:g.218881700_218881704delinsTTGTG	GRCh38
NC_000002.11:g.219746422_219746426delinsTTGTG , CM000664.1:g.219746422_219746426delinsTTGTG	GRCh37
NC_000002.10:g.219454666_219454670delinsTTGTG	NCBI36
NG_012179.1:g.6168_6172delinsTTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-461_114-457delinsTTGTG MANE Select	ENSP00000258411.3:n.114-461_114-457delinsTTGTG
ENST00000258411.7:c.114-461_114-457delinsTTGTG	ENSP00000258411.3:n.114-461_114-457delinsTTGTG
NM_025216.2:c.114-461_114-457delinsTTGTG	NP_079492.2:n.114-461_114-457delinsTTGTG
XM_011511928.1:c.62+233_62+237delinsTTGTG	XP_011510230.1:n.62+233_62+237delinsTTGTG
XM_011511929.1:c.18-461_18-457delinsTTGTG	XP_011510231.1:n.18-461_18-457delinsTTGTG
XM_011511930.1:c.114-461_114-457delinsTTGTG	XP_011510232.1:n.114-461_114-457delinsTTGTG
XM_011511929.2:c.18-461_18-457delinsTTGTG	XP_011510231.1:n.18-461_18-457delinsTTGTG
NM_025216.3:c.114-461_114-457delinsTTGTG MANE Select	NP_079492.2:n.114-461_114-457delinsTTGTG