Canonical Allele Identifier: CA354051335
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414377T>A , CM000665.2:g.119414377T>A GRCh38
NC_000003.11:g.119133224T>A , CM000665.1:g.119133224T>A GRCh37
NC_000003.10:g.120615914T>A NCBI36
NG_007665.2:g.125005T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2448T>A MANE Select ENSP00000264245.4:p.Asp816Glu
ENST00000264245.8:c.2448T>A ENSP00000264245.4:p.Asp816Glu
NM_020754.3:c.2448T>A NP_065805.2:p.Asp816Glu
XM_005247671.3:c.2355T>A XP_005247728.1:p.Asp785Glu
XM_006713714.2:c.2388T>A XP_006713777.1:p.Asp796Glu
XM_006713714.3:c.2388T>A XP_006713777.1:p.Asp796Glu
XM_017006955.1:c.1956T>A XP_016862444.1:p.Asp652Glu
NM_020754.4:c.2448T>A MANE Select NP_065805.2:p.Asp816Glu