Canonical Allele Identifier: CA2667116152

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119415082-GCACAGCAGTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119415088_119415097del , CM000665.2:g.119415088_119415097del	GRCh38
NC_000003.11:g.119133935_119133944del , CM000665.1:g.119133935_119133944del	GRCh37
NC_000003.10:g.120616625_120616634del	NCBI36
NG_007665.2:g.125716_125725del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.3159_3168del MANE Select	ENSP00000264245.4:p.Ser1053ArgfsTer?
ENST00000264245.8:c.3159_3168del	ENSP00000264245.4:p.Ser1053ArgfsTer?
NM_020754.3:c.3159_3168del	NP_065805.2:p.Ser1053ArgfsTer?
XM_005247671.3:c.3066_3075del	XP_005247728.1:p.Ser1022ArgfsTer?
XM_006713714.2:c.3099_3108del	XP_006713777.1:p.Ser1033ArgfsTer?
XM_006713714.3:c.3099_3108del	XP_006713777.1:p.Ser1033ArgfsTer?
XM_017006955.1:c.2667_2676del	XP_016862444.1:p.Ser889ArgfsTer?
NM_020754.4:c.3159_3168del MANE Select	NP_065805.2:p.Ser1053ArgfsTer?