Canonical Allele Identifier: CA435209484

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119402376-C-T
• MyVariant Identifiers: chr3:g.119121223C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119402376C>T , CM000665.2:g.119402376C>T	GRCh38
NC_000003.11:g.119121223C>T , CM000665.1:g.119121223C>T	GRCh37
NC_000003.10:g.120603913C>T	NCBI36
NG_007665.2:g.113004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1624C>T MANE Select	ENSP00000264245.4:p.Leu542=
ENST00000264245.8:c.1624C>T	ENSP00000264245.4:p.Leu542=
NM_020754.3:c.1624C>T	NP_065805.2:p.Leu542=
XM_005247671.3:c.1531C>T	XP_005247728.1:p.Leu511=
XM_006713714.2:c.1564C>T	XP_006713777.1:p.Leu522=
XM_006713714.3:c.1564C>T	XP_006713777.1:p.Leu522=
XM_017006955.1:c.1132C>T	XP_016862444.1:p.Leu378=
NM_020754.4:c.1624C>T MANE Select	NP_065805.2:p.Leu542=