Canonical Allele Identifier: CA354049698
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1313648676

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414123A>G , CM000665.2:g.119414123A>G GRCh38
NC_000003.11:g.119132970A>G , CM000665.1:g.119132970A>G GRCh37
NC_000003.10:g.120615660A>G NCBI36
NG_007665.2:g.124751A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2194A>G MANE Select ENSP00000264245.4:p.Thr732Ala
ENST00000264245.8:c.2194A>G ENSP00000264245.4:p.Thr732Ala
NM_020754.3:c.2194A>G NP_065805.2:p.Thr732Ala
XM_005247671.3:c.2101A>G XP_005247728.1:p.Thr701Ala
XM_006713714.2:c.2134A>G XP_006713777.1:p.Thr712Ala
XM_006713714.3:c.2134A>G XP_006713777.1:p.Thr712Ala
XM_017006955.1:c.1702A>G XP_016862444.1:p.Thr568Ala
NM_020754.4:c.2194A>G MANE Select NP_065805.2:p.Thr732Ala