Canonical Allele Identifier: CA81697656
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs34762342
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414342dup , CM000665.2:g.119414342dup GRCh38
NC_000003.11:g.119133189dup , CM000665.1:g.119133189dup GRCh37
NC_000003.10:g.120615879dup NCBI36
NG_007665.2:g.124970dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2413dup MANE Select ENSP00000264245.4:p.Glu805GlyfsTer25
ENST00000264245.8:c.2413dup ENSP00000264245.4:p.Glu805GlyfsTer25
NM_020754.3:c.2413dup NP_065805.2:p.Glu805GlyfsTer25
XM_005247671.3:c.2320dup XP_005247728.1:p.Glu774GlyfsTer25
XM_006713714.2:c.2353dup XP_006713777.1:p.Glu785GlyfsTer25
XM_006713714.3:c.2353dup XP_006713777.1:p.Glu785GlyfsTer25
XM_017006955.1:c.1921dup XP_016862444.1:p.Glu641GlyfsTer25
NM_020754.4:c.2413dup MANE Select NP_065805.2:p.Glu805GlyfsTer25
Search 100 bp 5'
Search 100 bp 3'