Canonical Allele Identifier: CA2113842
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs745898676
ExAC: 2:219746917 C / A
gnomAD v2: 2-219746917-C-A
gnomAD v3: 2-218882195-C-A
gnomAD v4: 2-218882195-C-A
MyVariant Identifiers: chr2:g.219746917C>A (hg19) chr2:g.218882195C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882195C>A , CM000664.2:g.218882195C>A GRCh38
NC_000002.11:g.219746917C>A , CM000664.1:g.219746917C>A GRCh37
NC_000002.10:g.219455161C>A NCBI36
NG_012179.1:g.6663C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.148C>A MANE Select ENSP00000258411.3:p.Pro50Thr
ENST00000258411.7:c.148C>A ENSP00000258411.3:p.Pro50Thr
ENST00000458582.1:c.35C>A
NM_025216.2:c.148C>A NP_079492.2:p.Pro50Thr
XM_011511928.1:c.97C>A XP_011510230.1:p.Pro33Thr
XM_011511929.1:c.52C>A XP_011510231.1:p.Pro18Thr
XM_011511930.1:c.148C>A XP_011510232.1:p.Pro50Thr
XM_011511929.2:c.52C>A XP_011510231.1:p.Pro18Thr
NM_025216.3:c.148C>A MANE Select NP_079492.2:p.Pro50Thr
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