Canonical Allele Identifier: CA350592382
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757926T>C (hg19) chr2:g.218893204T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893204T>C , CM000664.2:g.218893204T>C GRCh38
NC_000002.11:g.219757926T>C , CM000664.1:g.219757926T>C GRCh37
NC_000002.10:g.219466170T>C NCBI36
NG_012179.1:g.17672T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1187T>C MANE Select ENSP00000258411.3:p.Phe396Ser
ENST00000258411.7:c.1187T>C ENSP00000258411.3:p.Phe396Ser
NM_025216.2:c.1187T>C NP_079492.2:p.Phe396Ser
XM_011511928.1:c.1136T>C XP_011510230.1:p.Phe379Ser
XM_011511929.1:c.1091T>C XP_011510231.1:p.Phe364Ser
XM_011511930.1:c.807T>C XP_011510232.1:p.Leu269=
XM_011511929.2:c.1091T>C XP_011510231.1:p.Phe364Ser
NM_025216.3:c.1187T>C MANE Select NP_079492.2:p.Phe396Ser
Search 100 bp 5'
Search 100 bp 3'