Canonical Allele Identifier: CA354051551
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414415A>T , CM000665.2:g.119414415A>T GRCh38
NC_000003.11:g.119133262A>T , CM000665.1:g.119133262A>T GRCh37
NC_000003.10:g.120615952A>T NCBI36
NG_007665.2:g.125043A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2486A>T MANE Select ENSP00000264245.4:p.Glu829Val
ENST00000264245.8:c.2486A>T ENSP00000264245.4:p.Glu829Val
NM_020754.3:c.2486A>T NP_065805.2:p.Glu829Val
XM_005247671.3:c.2393A>T XP_005247728.1:p.Glu798Val
XM_006713714.2:c.2426A>T XP_006713777.1:p.Glu809Val
XM_006713714.3:c.2426A>T XP_006713777.1:p.Glu809Val
XM_017006955.1:c.1994A>T XP_016862444.1:p.Glu665Val
NM_020754.4:c.2486A>T MANE Select NP_065805.2:p.Glu829Val