Canonical Allele Identifier: CA354051604

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133270A>T (hg19) ; chr3:g.119414423A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414423A>T , CM000665.2:g.119414423A>T	GRCh38
NC_000003.11:g.119133270A>T , CM000665.1:g.119133270A>T	GRCh37
NC_000003.10:g.120615960A>T	NCBI36
NG_007665.2:g.125051A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2494A>T MANE Select	ENSP00000264245.4:p.Ser832Cys
ENST00000264245.8:c.2494A>T	ENSP00000264245.4:p.Ser832Cys
NM_020754.3:c.2494A>T	NP_065805.2:p.Ser832Cys
XM_005247671.3:c.2401A>T	XP_005247728.1:p.Ser801Cys
XM_006713714.2:c.2434A>T	XP_006713777.1:p.Ser812Cys
XM_006713714.3:c.2434A>T	XP_006713777.1:p.Ser812Cys
XM_017006955.1:c.2002A>T	XP_016862444.1:p.Ser668Cys
NM_020754.4:c.2494A>T MANE Select	NP_065805.2:p.Ser832Cys