Canonical Allele Identifier: CA350618537
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1575229926

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882262T>G , CM000664.2:g.218882262T>G GRCh38
NC_000002.11:g.219746984T>G , CM000664.1:g.219746984T>G GRCh37
NC_000002.10:g.219455228T>G NCBI36
NG_012179.1:g.6730T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.215T>G MANE Select ENSP00000258411.3:p.Met72Arg
ENST00000258411.7:c.215T>G ENSP00000258411.3:p.Met72Arg
ENST00000458582.1:c.102T>G
NM_025216.2:c.215T>G NP_079492.2:p.Met72Arg
XM_011511928.1:c.164T>G XP_011510230.1:p.Met55Arg
XM_011511929.1:c.119T>G XP_011510231.1:p.Met40Arg
XM_011511930.1:c.215T>G XP_011510232.1:p.Met72Arg
XM_011511929.2:c.119T>G XP_011510231.1:p.Met40Arg
NM_025216.3:c.215T>G MANE Select NP_079492.2:p.Met72Arg