Canonical Allele Identifier: CA350592312
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893198G>T , CM000664.2:g.218893198G>T GRCh38
NC_000002.11:g.219757920G>T , CM000664.1:g.219757920G>T GRCh37
NC_000002.10:g.219466164G>T NCBI36
NG_012179.1:g.17666G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1181G>T MANE Select ENSP00000258411.3:p.Cys394Phe
ENST00000258411.7:c.1181G>T ENSP00000258411.3:p.Cys394Phe
NM_025216.2:c.1181G>T NP_079492.2:p.Cys394Phe
XM_011511928.1:c.1130G>T XP_011510230.1:p.Cys377Phe
XM_011511929.1:c.1085G>T XP_011510231.1:p.Cys362Phe
XM_011511930.1:c.801G>T XP_011510232.1:p.Leu267=
XM_011511929.2:c.1085G>T XP_011510231.1:p.Cys362Phe
NM_025216.3:c.1181G>T MANE Select NP_079492.2:p.Cys394Phe