Canonical Allele Identifier: CA2553994
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs751198282

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414183C>G , CM000665.2:g.119414183C>G GRCh38
NC_000003.11:g.119133030C>G , CM000665.1:g.119133030C>G GRCh37
NC_000003.10:g.120615720C>G NCBI36
NG_007665.2:g.124811C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2254C>G MANE Select ENSP00000264245.4:p.Leu752Val
ENST00000264245.8:c.2254C>G ENSP00000264245.4:p.Leu752Val
NM_020754.3:c.2254C>G NP_065805.2:p.Leu752Val
XM_005247671.3:c.2161C>G XP_005247728.1:p.Leu721Val
XM_006713714.2:c.2194C>G XP_006713777.1:p.Leu732Val
XM_006713714.3:c.2194C>G XP_006713777.1:p.Leu732Val
XM_017006955.1:c.1762C>G XP_016862444.1:p.Leu588Val
NM_020754.4:c.2254C>G MANE Select NP_065805.2:p.Leu752Val