Canonical Allele Identifier: CA354050456
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414239A>T , CM000665.2:g.119414239A>T GRCh38
NC_000003.11:g.119133086A>T , CM000665.1:g.119133086A>T GRCh37
NC_000003.10:g.120615776A>T NCBI36
NG_007665.2:g.124867A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2310A>T MANE Select ENSP00000264245.4:p.Glu770Asp
ENST00000264245.8:c.2310A>T ENSP00000264245.4:p.Glu770Asp
NM_020754.3:c.2310A>T NP_065805.2:p.Glu770Asp
XM_005247671.3:c.2217A>T XP_005247728.1:p.Glu739Asp
XM_006713714.2:c.2250A>T XP_006713777.1:p.Glu750Asp
XM_006713714.3:c.2250A>T XP_006713777.1:p.Glu750Asp
XM_017006955.1:c.1818A>T XP_016862444.1:p.Glu606Asp
NM_020754.4:c.2310A>T MANE Select NP_065805.2:p.Glu770Asp