Canonical Allele Identifier: CA354049465

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119132929G>T (hg19) ; chr3:g.119414082G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414082G>T , CM000665.2:g.119414082G>T	GRCh38
NC_000003.11:g.119132929G>T , CM000665.1:g.119132929G>T	GRCh37
NC_000003.10:g.120615619G>T	NCBI36
NG_007665.2:g.124710G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2153G>T MANE Select	ENSP00000264245.4:p.Trp718Leu
ENST00000264245.8:c.2153G>T	ENSP00000264245.4:p.Trp718Leu
NM_020754.3:c.2153G>T	NP_065805.2:p.Trp718Leu
XM_005247671.3:c.2060G>T	XP_005247728.1:p.Trp687Leu
XM_006713714.2:c.2093G>T	XP_006713777.1:p.Trp698Leu
XM_006713714.3:c.2093G>T	XP_006713777.1:p.Trp698Leu
XM_017006955.1:c.1661G>T	XP_016862444.1:p.Trp554Leu
NM_020754.4:c.2153G>T MANE Select	NP_065805.2:p.Trp718Leu