Canonical Allele Identifier: CA2663173466
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218882270-T-TGTGTGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882273_218882278dup , CM000664.2:g.218882273_218882278dup GRCh38
NC_000002.11:g.219746995_219747000dup , CM000664.1:g.219746995_219747000dup GRCh37
NC_000002.10:g.219455239_219455244dup NCBI36
NG_012179.1:g.6741_6746dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.226_231dup MANE Select ENSP00000258411.3:p.Arg77_His78insValArg
ENST00000258411.7:c.226_231dup ENSP00000258411.3:p.Arg77_His78insValArg
ENST00000458582.1:c.113_118dup
NM_025216.2:c.226_231dup NP_079492.2:p.Arg77_His78insValArg
XM_011511928.1:c.175_180dup XP_011510230.1:p.Arg60_His61insValArg
XM_011511929.1:c.130_135dup XP_011510231.1:p.Arg45_His46insValArg
XM_011511930.1:c.226_231dup XP_011510232.1:p.Arg77_His78insValArg
XM_011511929.2:c.130_135dup XP_011510231.1:p.Arg45_His46insValArg
NM_025216.3:c.226_231dup MANE Select NP_079492.2:p.Arg77_His78insValArg
Search 100 bp 5'
Search 100 bp 3'