Canonical Allele Identifier: CA350586966
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219754980C>A (hg19) chr2:g.218890258C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218890258C>A , CM000664.2:g.218890258C>A GRCh38
NC_000002.11:g.219754980C>A , CM000664.1:g.219754980C>A GRCh37
NC_000002.10:g.219463224C>A NCBI36
NG_012179.1:g.14726C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.651C>A MANE Select ENSP00000258411.3:p.Asp217Glu
ENST00000258411.7:c.651C>A ENSP00000258411.3:p.Asp217Glu
ENST00000458582.1:c.264-2516C>A
NM_025216.2:c.651C>A NP_079492.2:p.Asp217Glu
XM_011511928.1:c.600C>A XP_011510230.1:p.Asp200Glu
XM_011511929.1:c.555C>A XP_011510231.1:p.Asp185Glu
XM_011511930.1:c.377-2516C>A XP_011510232.1:n.377-2516C>A
XM_011511929.2:c.555C>A XP_011510231.1:p.Asp185Glu
NM_025216.3:c.651C>A MANE Select NP_079492.2:p.Asp217Glu
Search 100 bp 5'
Search 100 bp 3'