Canonical Allele Identifier: CA1396548678

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414382A= , CM000665.2:g.119414382A=	GRCh38
NC_000003.11:g.119133229A= , CM000665.1:g.119133229A=	GRCh37
NC_000003.10:g.120615919A=	NCBI36
NG_007665.2:g.125010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2453A= MANE Select	ENSP00000264245.4:p.Tyr818=
ENST00000264245.8:c.2453A=	ENSP00000264245.4:p.Tyr818=
NM_020754.3:c.2453A=	NP_065805.2:p.Tyr818=
XM_005247671.3:c.2360A=	XP_005247728.1:p.Tyr787=
XM_006713714.2:c.2393A=	XP_006713777.1:p.Tyr798=
XM_006713714.3:c.2393A=	XP_006713777.1:p.Tyr798=
XM_017006955.1:c.1961A=	XP_016862444.1:p.Tyr654=
NM_020754.4:c.2453A= MANE Select	NP_065805.2:p.Tyr818=