Canonical Allele Identifier: CA1396548495
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413976C= , CM000665.2:g.119413976C= GRCh38
NC_000003.11:g.119132823C= , CM000665.1:g.119132823C= GRCh37
NC_000003.10:g.120615513C= NCBI36
NG_007665.2:g.124604C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.2047C= MANE Select ENSP00000264245.4:p.Gln683=
ENST00000264245.8:c.2047C= ENSP00000264245.4:p.Gln683=
NM_020754.3:c.2047C= NP_065805.2:p.Gln683=
XM_005247671.3:c.1954C= XP_005247728.1:p.Gln652=
XM_006713714.2:c.1987C= XP_006713777.1:p.Gln663=
XM_006713714.3:c.1987C= XP_006713777.1:p.Gln663=
XM_017006955.1:c.1555C= XP_016862444.1:p.Gln519=
NM_020754.4:c.2047C= MANE Select NP_065805.2:p.Gln683=