Canonical Allele Identifier: CA2663174566
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893277-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893277C>T , CM000664.2:g.218893277C>T GRCh38
NC_000002.11:g.219757999C>T , CM000664.1:g.219757999C>T GRCh37
NC_000002.10:g.219466243C>T NCBI36
NG_012179.1:g.17745C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.*6C>T MANE Select ENSP00000258411.3:n.*6C>T
ENST00000258411.7:c.*6C>T ENSP00000258411.3:n.*6C>T
ENST00000489887.1:n.47+10C>T
NM_025216.2:c.*6C>T NP_079492.2:n.*6C>T
XM_011511928.1:c.*6C>T XP_011510230.1:n.*6C>T
XM_011511929.1:c.*6C>T XP_011510231.1:n.*6C>T
XM_011511930.1:c.880C>T XP_011510232.1:p.Pro294Ser
XM_011511929.2:c.*6C>T XP_011510231.1:n.*6C>T
NM_025216.3:c.*6C>T MANE Select NP_079492.2:n.*6C>T
Search 100 bp 5'
Search 100 bp 3'