Canonical Allele Identifier: CA354047762

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119413867-T-G
• MyVariant Identifiers: chr3:g.119132714T>G (hg19) ; chr3:g.119413867T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413867T>G , CM000665.2:g.119413867T>G	GRCh38
NC_000003.11:g.119132714T>G , CM000665.1:g.119132714T>G	GRCh37
NC_000003.10:g.120615404T>G	NCBI36
NG_007665.2:g.124495T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1938T>G MANE Select	ENSP00000264245.4:p.Asp646Glu
ENST00000264245.8:c.1938T>G	ENSP00000264245.4:p.Asp646Glu
NM_020754.3:c.1938T>G	NP_065805.2:p.Asp646Glu
XM_005247671.3:c.1845T>G	XP_005247728.1:p.Asp615Glu
XM_006713714.2:c.1878T>G	XP_006713777.1:p.Asp626Glu
XM_006713714.3:c.1878T>G	XP_006713777.1:p.Asp626Glu
XM_017006955.1:c.1446T>G	XP_016862444.1:p.Asp482Glu
NM_020754.4:c.1938T>G MANE Select	NP_065805.2:p.Asp646Glu