Canonical Allele Identifier: CA350592151
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893182-A-C
MyVariant Identifiers: chr2:g.219757904A>C (hg19) chr2:g.218893182A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893182A>C , CM000664.2:g.218893182A>C GRCh38
NC_000002.11:g.219757904A>C , CM000664.1:g.219757904A>C GRCh37
NC_000002.10:g.219466148A>C NCBI36
NG_012179.1:g.17650A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1165A>C MANE Select ENSP00000258411.3:p.Ser389Arg
ENST00000258411.7:c.1165A>C ENSP00000258411.3:p.Ser389Arg
NM_025216.2:c.1165A>C NP_079492.2:p.Ser389Arg
XM_011511928.1:c.1114A>C XP_011510230.1:p.Ser372Arg
XM_011511929.1:c.1069A>C XP_011510231.1:p.Ser357Arg
XM_011511930.1:c.785A>C XP_011510232.1:p.Gln262Pro
XM_011511929.2:c.1069A>C XP_011510231.1:p.Ser357Arg
NM_025216.3:c.1165A>C MANE Select NP_079492.2:p.Ser389Arg
Search 100 bp 5'
Search 100 bp 3'