Canonical Allele Identifier: CA350592610
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757950G>C (hg19) chr2:g.218893228G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893228G>C , CM000664.2:g.218893228G>C GRCh38
NC_000002.11:g.219757950G>C , CM000664.1:g.219757950G>C GRCh37
NC_000002.10:g.219466194G>C NCBI36
NG_012179.1:g.17696G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1211G>C MANE Select ENSP00000258411.3:p.Cys404Ser
ENST00000258411.7:c.1211G>C ENSP00000258411.3:p.Cys404Ser
ENST00000489887.1:n.8G>C
NM_025216.2:c.1211G>C NP_079492.2:p.Cys404Ser
XM_011511928.1:c.1160G>C XP_011510230.1:p.Cys387Ser
XM_011511929.1:c.1115G>C XP_011510231.1:p.Cys372Ser
XM_011511930.1:c.831G>C XP_011510232.1:p.Leu277=
XM_011511929.2:c.1115G>C XP_011510231.1:p.Cys372Ser
NM_025216.3:c.1211G>C MANE Select NP_079492.2:p.Cys404Ser
Search 100 bp 5'
Search 100 bp 3'