Canonical Allele Identifier: CA1328961539
Gene: WNT10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882218_218882219delinsCA , CM000664.2:g.218882218_218882219delinsCA GRCh38
NC_000002.11:g.219746940_219746941delinsCA , CM000664.1:g.219746940_219746941delinsCA GRCh37
NC_000002.10:g.219455184_219455185delinsCA NCBI36
NG_012179.1:g.6686_6687delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.171_172delinsCA MANE Select ENSP00000258411.3:p.Ala57=
ENST00000258411.7:c.171_172delinsCA ENSP00000258411.3:p.Ala57=
ENST00000458582.1:c.58_59delinsCA
NM_025216.2:c.171_172delinsCA NP_079492.2:p.Ala57=
XM_011511928.1:c.120_121delinsCA XP_011510230.1:p.Ala40=
XM_011511929.1:c.75_76delinsCA XP_011510231.1:p.Ala25=
XM_011511930.1:c.171_172delinsCA XP_011510232.1:p.Ala57=
XM_011511929.2:c.75_76delinsCA XP_011510231.1:p.Ala25=
NM_025216.3:c.171_172delinsCA MANE Select NP_079492.2:p.Ala57=