Canonical Allele Identifier: CA354048194

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119132775G>T (hg19) ; chr3:g.119413928G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413928G>T , CM000665.2:g.119413928G>T	GRCh38
NC_000003.11:g.119132775G>T , CM000665.1:g.119132775G>T	GRCh37
NC_000003.10:g.120615465G>T	NCBI36
NG_007665.2:g.124556G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1999G>T MANE Select	ENSP00000264245.4:p.Glu667Ter
ENST00000264245.8:c.1999G>T	ENSP00000264245.4:p.Glu667Ter
NM_020754.3:c.1999G>T	NP_065805.2:p.Glu667Ter
XM_005247671.3:c.1906G>T	XP_005247728.1:p.Glu636Ter
XM_006713714.2:c.1939G>T	XP_006713777.1:p.Glu647Ter
XM_006713714.3:c.1939G>T	XP_006713777.1:p.Glu647Ter
XM_017006955.1:c.1507G>T	XP_016862444.1:p.Glu503Ter
NM_020754.4:c.1999G>T MANE Select	NP_065805.2:p.Glu667Ter