Canonical Allele Identifier: CA354050647

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133117C>G (hg19) ; chr3:g.119414270C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414270C>G , CM000665.2:g.119414270C>G	GRCh38
NC_000003.11:g.119133117C>G , CM000665.1:g.119133117C>G	GRCh37
NC_000003.10:g.120615807C>G	NCBI36
NG_007665.2:g.124898C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2341C>G MANE Select	ENSP00000264245.4:p.Leu781Val
ENST00000264245.8:c.2341C>G	ENSP00000264245.4:p.Leu781Val
NM_020754.3:c.2341C>G	NP_065805.2:p.Leu781Val
XM_005247671.3:c.2248C>G	XP_005247728.1:p.Leu750Val
XM_006713714.2:c.2281C>G	XP_006713777.1:p.Leu761Val
XM_006713714.3:c.2281C>G	XP_006713777.1:p.Leu761Val
XM_017006955.1:c.1849C>G	XP_016862444.1:p.Leu617Val
NM_020754.4:c.2341C>G MANE Select	NP_065805.2:p.Leu781Val