Canonical Allele Identifier: CA350586983
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219754983G>C (hg19) chr2:g.218890261G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218890261G>C , CM000664.2:g.218890261G>C GRCh38
NC_000002.11:g.219754983G>C , CM000664.1:g.219754983G>C GRCh37
NC_000002.10:g.219463227G>C NCBI36
NG_012179.1:g.14729G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.654G>C MANE Select ENSP00000258411.3:p.Met218Ile
ENST00000258411.7:c.654G>C ENSP00000258411.3:p.Met218Ile
ENST00000458582.1:c.264-2513G>C
NM_025216.2:c.654G>C NP_079492.2:p.Met218Ile
XM_011511928.1:c.603G>C XP_011510230.1:p.Met201Ile
XM_011511929.1:c.558G>C XP_011510231.1:p.Met186Ile
XM_011511930.1:c.377-2513G>C XP_011510232.1:n.377-2513G>C
XM_011511929.2:c.558G>C XP_011510231.1:p.Met186Ile
NM_025216.3:c.654G>C MANE Select NP_079492.2:p.Met218Ile
Search 100 bp 5'
Search 100 bp 3'