Canonical Allele Identifier: CA1396548987

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119415186_119415187delinsCA , CM000665.2:g.119415186_119415187delinsCA	GRCh38
NC_000003.11:g.119134033_119134034delinsCA , CM000665.1:g.119134033_119134034delinsCA	GRCh37
NC_000003.10:g.120616723_120616724delinsCA	NCBI36
NG_007665.2:g.125814_125815delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.3257_3258delinsCA MANE Select	ENSP00000264245.4:p.Ala1086=
ENST00000264245.8:c.3257_3258delinsCA	ENSP00000264245.4:p.Ala1086=
NM_020754.3:c.3257_3258delinsCA	NP_065805.2:p.Ala1086=
XM_005247671.3:c.3164_3165delinsCA	XP_005247728.1:p.Ala1055=
XM_006713714.2:c.3197_3198delinsCA	XP_006713777.1:p.Ala1066=
XM_006713714.3:c.3197_3198delinsCA	XP_006713777.1:p.Ala1066=
XM_017006955.1:c.2765_2766delinsCA	XP_016862444.1:p.Ala922=
NM_020754.4:c.3257_3258delinsCA MANE Select	NP_065805.2:p.Ala1086=