Canonical Allele Identifier: CA350592920
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757992G>C (hg19) chr2:g.218893270G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893270G>C , CM000664.2:g.218893270G>C GRCh38
NC_000002.11:g.219757992G>C , CM000664.1:g.219757992G>C GRCh37
NC_000002.10:g.219466236G>C NCBI36
NG_012179.1:g.17738G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1253G>C MANE Select ENSP00000258411.3:p.Ter418Ser
ENST00000258411.7:c.1253G>C ENSP00000258411.3:p.Ter418Ser
ENST00000489887.1:n.47+3G>C
NM_025216.2:c.1253G>C NP_079492.2:p.Ter418Ser
XM_011511928.1:c.1202G>C XP_011510230.1:p.Ter401Ser
XM_011511929.1:c.1157G>C XP_011510231.1:p.Ter386Ser
XM_011511930.1:c.873G>C XP_011510232.1:p.Val291=
XM_011511929.2:c.1157G>C XP_011510231.1:p.Ter386Ser
NM_025216.3:c.1253G>C MANE Select NP_079492.2:p.Ter418Ser
Search 100 bp 5'
Search 100 bp 3'