Canonical Allele Identifier: CA1328965621
Gene: WNT10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893217T= , CM000664.2:g.218893217T= GRCh38
NC_000002.11:g.219757939T= , CM000664.1:g.219757939T= GRCh37
NC_000002.10:g.219466183T= NCBI36
NG_012179.1:g.17685T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1200T= MANE Select ENSP00000258411.3:p.Cys400=
ENST00000258411.7:c.1200T= ENSP00000258411.3:p.Cys400=
NM_025216.2:c.1200T= NP_079492.2:p.Cys400=
XM_011511928.1:c.1149T= XP_011510230.1:p.Cys383=
XM_011511929.1:c.1104T= XP_011510231.1:p.Cys368=
XM_011511930.1:c.820T= XP_011510232.1:p.Phe274=
XM_011511929.2:c.1104T= XP_011510231.1:p.Cys368=
NM_025216.3:c.1200T= MANE Select NP_079492.2:p.Cys400=