Canonical Allele Identifier: CA1139657705

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 966598
• ClinVar RCV Id: RCV001241317
• dbSNP Id: rs1944678383

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893182_218893195delinsTTCCAGCACAACATC , CM000664.2:g.218893182_218893195delinsTTCCAGCACAACATC	GRCh38
NC_000002.11:g.219757904_219757917delinsTTCCAGCACAACATC , CM000664.1:g.219757904_219757917delinsTTCCAGCACAACATC	GRCh37
NC_000002.10:g.219466148_219466161delinsTTCCAGCACAACATC	NCBI36
NG_012179.1:g.17650_17663delinsTTCCAGCACAACATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1165_1178delinsTTCCAGCACAACATC MANE Select	ENSP00000258411.3:p.Ser389PhefsTer?
ENST00000258411.7:c.1165_1178delinsTTCCAGCACAACATC	ENSP00000258411.3:p.Ser389PhefsTer?
NM_025216.2:c.1165_1178delinsTTCCAGCACAACATC	NP_079492.2:p.Ser389PhefsTer?
XM_011511928.1:c.1114_1127delinsTTCCAGCACAACATC	XP_011510230.1:p.Ser372PhefsTer?
XM_011511929.1:c.1069_1082delinsTTCCAGCACAACATC	XP_011510231.1:p.Ser357PhefsTer?
XM_011511930.1:c.785_798delinsTTCCAGCACAACATC	XP_011510232.1:p.Gln262LeufsTer?
XM_011511929.2:c.1069_1082delinsTTCCAGCACAACATC	XP_011510231.1:p.Ser357PhefsTer?
NM_025216.3:c.1165_1178delinsTTCCAGCACAACATC MANE Select	NP_079492.2:p.Ser389PhefsTer?