Canonical Allele Identifier: CA2758107662

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119415186_119415187del , CM000665.2:g.119415186_119415187del	GRCh38
NC_000003.11:g.119134033_119134034del , CM000665.1:g.119134033_119134034del	GRCh37
NC_000003.10:g.120616723_120616724del	NCBI36
NG_007665.2:g.125814_125815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.3257_3258del MANE Select	ENSP00000264245.4:p.Ala1086GlufsTer?
ENST00000264245.8:c.3257_3258del	ENSP00000264245.4:p.Ala1086GlufsTer?
NM_020754.3:c.3257_3258del	NP_065805.2:p.Ala1086GlufsTer?
XM_005247671.3:c.3164_3165del	XP_005247728.1:p.Ala1055GlufsTer?
XM_006713714.2:c.3197_3198del	XP_006713777.1:p.Ala1066GlufsTer?
XM_006713714.3:c.3197_3198del	XP_006713777.1:p.Ala1066GlufsTer?
XM_017006955.1:c.2765_2766del	XP_016862444.1:p.Ala922GlufsTer?
NM_020754.4:c.3257_3258del MANE Select	NP_065805.2:p.Ala1086GlufsTer?