Canonical Allele Identifier: CA1396548689

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414409G= , CM000665.2:g.119414409G=	GRCh38
NC_000003.11:g.119133256G= , CM000665.1:g.119133256G=	GRCh37
NC_000003.10:g.120615946G=	NCBI36
NG_007665.2:g.125037G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2480G= MANE Select	ENSP00000264245.4:p.Ser827=
ENST00000264245.8:c.2480G=	ENSP00000264245.4:p.Ser827=
NM_020754.3:c.2480G=	NP_065805.2:p.Ser827=
XM_005247671.3:c.2387G=	XP_005247728.1:p.Ser796=
XM_006713714.2:c.2420G=	XP_006713777.1:p.Ser807=
XM_006713714.3:c.2420G=	XP_006713777.1:p.Ser807=
XM_017006955.1:c.1988G=	XP_016862444.1:p.Ser663=
NM_020754.4:c.2480G= MANE Select	NP_065805.2:p.Ser827=