Canonical Allele Identifier: CA2577942208

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413993_119413997del , CM000665.2:g.119413993_119413997del	GRCh38
NC_000003.11:g.119132840_119132844del , CM000665.1:g.119132840_119132844del	GRCh37
NC_000003.10:g.120615530_120615534del	NCBI36
NG_007665.2:g.124621_124625del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2064_2068del MANE Select	ENSP00000264245.4:p.Ser689GlyfsTer?
ENST00000264245.8:c.2064_2068del	ENSP00000264245.4:p.Ser689GlyfsTer?
NM_020754.3:c.2064_2068del	NP_065805.2:p.Ser689GlyfsTer?
XM_005247671.3:c.1971_1975del	XP_005247728.1:p.Ser658GlyfsTer?
XM_006713714.2:c.2004_2008del	XP_006713777.1:p.Ser669GlyfsTer?
XM_006713714.3:c.2004_2008del	XP_006713777.1:p.Ser669GlyfsTer?
XM_017006955.1:c.1572_1576del	XP_016862444.1:p.Ser525GlyfsTer?
NM_020754.4:c.2064_2068del MANE Select	NP_065805.2:p.Ser689GlyfsTer?