Canonical Allele Identifier: CA354051682
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1263353833

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414436G>C , CM000665.2:g.119414436G>C GRCh38
NC_000003.11:g.119133283G>C , CM000665.1:g.119133283G>C GRCh37
NC_000003.10:g.120615973G>C NCBI36
NG_007665.2:g.125064G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2507G>C MANE Select ENSP00000264245.4:p.Gly836Ala
ENST00000264245.8:c.2507G>C ENSP00000264245.4:p.Gly836Ala
NM_020754.3:c.2507G>C NP_065805.2:p.Gly836Ala
XM_005247671.3:c.2414G>C XP_005247728.1:p.Gly805Ala
XM_006713714.2:c.2447G>C XP_006713777.1:p.Gly816Ala
XM_006713714.3:c.2447G>C XP_006713777.1:p.Gly816Ala
XM_017006955.1:c.2015G>C XP_016862444.1:p.Gly672Ala
NM_020754.4:c.2507G>C MANE Select NP_065805.2:p.Gly836Ala