Canonical Allele Identifier: CA435411564
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119132900T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414053T>A , CM000665.2:g.119414053T>A GRCh38
NC_000003.11:g.119132900T>A , CM000665.1:g.119132900T>A GRCh37
NC_000003.10:g.120615590T>A NCBI36
NG_007665.2:g.124681T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2124T>A MANE Select ENSP00000264245.4:p.Pro708=
ENST00000264245.8:c.2124T>A ENSP00000264245.4:p.Pro708=
NM_020754.3:c.2124T>A NP_065805.2:p.Pro708=
XM_005247671.3:c.2031T>A XP_005247728.1:p.Pro677=
XM_006713714.2:c.2064T>A XP_006713777.1:p.Pro688=
XM_006713714.3:c.2064T>A XP_006713777.1:p.Pro688=
XM_017006955.1:c.1632T>A XP_016862444.1:p.Pro544=
NM_020754.4:c.2124T>A MANE Select NP_065805.2:p.Pro708=