Canonical Allele Identifier: CA1396548650
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414319T= , CM000665.2:g.119414319T= GRCh38
NC_000003.11:g.119133166T= , CM000665.1:g.119133166T= GRCh37
NC_000003.10:g.120615856T= NCBI36
NG_007665.2:g.124947T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2390T= MANE Select ENSP00000264245.4:p.Val797=
ENST00000264245.8:c.2390T= ENSP00000264245.4:p.Val797=
NM_020754.3:c.2390T= NP_065805.2:p.Val797=
XM_005247671.3:c.2297T= XP_005247728.1:p.Val766=
XM_006713714.2:c.2330T= XP_006713777.1:p.Val777=
XM_006713714.3:c.2330T= XP_006713777.1:p.Val777=
XM_017006955.1:c.1898T= XP_016862444.1:p.Val633=
NM_020754.4:c.2390T= MANE Select NP_065805.2:p.Val797=