Canonical Allele Identifier: CA2667110274

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119414419-CTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414420_119414422del , CM000665.2:g.119414420_119414422del	GRCh38
NC_000003.11:g.119133267_119133269del , CM000665.1:g.119133267_119133269del	GRCh37
NC_000003.10:g.120615957_120615959del	NCBI36
NG_007665.2:g.125048_125050del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2491_2493del MANE Select	ENSP00000264245.4:p.Ser831del
ENST00000264245.8:c.2491_2493del	ENSP00000264245.4:p.Ser831del
NM_020754.3:c.2491_2493del	NP_065805.2:p.Ser831del
XM_005247671.3:c.2398_2400del	XP_005247728.1:p.Ser800del
XM_006713714.2:c.2431_2433del	XP_006713777.1:p.Ser811del
XM_006713714.3:c.2431_2433del	XP_006713777.1:p.Ser811del
XM_017006955.1:c.1999_2001del	XP_016862444.1:p.Ser667del
NM_020754.4:c.2491_2493del MANE Select	NP_065805.2:p.Ser831del