Canonical Allele Identifier: CA354051249

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133213T>G (hg19) ; chr3:g.119414366T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414366T>G , CM000665.2:g.119414366T>G	GRCh38
NC_000003.11:g.119133213T>G , CM000665.1:g.119133213T>G	GRCh37
NC_000003.10:g.120615903T>G	NCBI36
NG_007665.2:g.124994T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2437T>G MANE Select	ENSP00000264245.4:p.Leu813Val
ENST00000264245.8:c.2437T>G	ENSP00000264245.4:p.Leu813Val
NM_020754.3:c.2437T>G	NP_065805.2:p.Leu813Val
XM_005247671.3:c.2344T>G	XP_005247728.1:p.Leu782Val
XM_006713714.2:c.2377T>G	XP_006713777.1:p.Leu793Val
XM_006713714.3:c.2377T>G	XP_006713777.1:p.Leu793Val
XM_017006955.1:c.1945T>G	XP_016862444.1:p.Leu649Val
NM_020754.4:c.2437T>G MANE Select	NP_065805.2:p.Leu813Val