Canonical Allele Identifier: CA1328961305

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881706_218881712delinsGTGTGTC , CM000664.2:g.218881706_218881712delinsGTGTGTC	GRCh38
NC_000002.11:g.219746428_219746434delinsGTGTGTC , CM000664.1:g.219746428_219746434delinsGTGTGTC	GRCh37
NC_000002.10:g.219454672_219454678delinsGTGTGTC	NCBI36
NG_012179.1:g.6174_6180delinsGTGTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-455_114-449delinsGTGTGTC MANE Select	ENSP00000258411.3:n.114-455_114-449delinsGTGTGTC
ENST00000258411.7:c.114-455_114-449delinsGTGTGTC	ENSP00000258411.3:n.114-455_114-449delinsGTGTGTC
NM_025216.2:c.114-455_114-449delinsGTGTGTC	NP_079492.2:n.114-455_114-449delinsGTGTGTC
XM_011511928.1:c.62+239_62+245delinsGTGTGTC	XP_011510230.1:n.62+239_62+245delinsGTGTGTC
XM_011511929.1:c.18-455_18-449delinsGTGTGTC	XP_011510231.1:n.18-455_18-449delinsGTGTGTC
XM_011511930.1:c.114-455_114-449delinsGTGTGTC	XP_011510232.1:n.114-455_114-449delinsGTGTGTC
XM_011511929.2:c.18-455_18-449delinsGTGTGTC	XP_011510231.1:n.18-455_18-449delinsGTGTGTC
NM_025216.3:c.114-455_114-449delinsGTGTGTC MANE Select	NP_079492.2:n.114-455_114-449delinsGTGTGTC