Canonical Allele Identifier: CA187711113

Gene: ARHGAP39

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144533250C>T , CM000670.2:g.144533250C>T	GRCh38
NC_000008.10:g.145758634C>T , CM000670.1:g.145758634C>T	GRCh37
NC_000008.9:g.145729442C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025251.3:c.2764G>A MANE Select	NP_079527.1:p.Ala922Thr
ENST00000377307.7:c.2764G>A MANE Select	ENSP00000366522.2:p.Ala922Thr
NM_001308207.1:c.2671G>A	NP_001295136.1:p.Ala891Thr
NM_001308208.1:c.2671G>A	NP_001295137.1:p.Ala891Thr
NM_001308208.2:c.2671G>A	NP_001295137.1:p.Ala891Thr
NM_025251.1:c.2764G>A	NP_079527.1:p.Ala922Thr
NM_025251.2:c.2764G>A	NP_079527.1:p.Ala922Thr
ENST00000276826.5:c.2671G>A	ENSP00000276826.5:p.Ala891Thr
ENST00000377307.6:c.2764G>A	ENSP00000366522.2:p.Ala922Thr
XM_011517308.1:c.2764G>A	XP_011515610.1:p.Ala922Thr
XM_011517309.1:c.2764G>A	XP_011515611.1:p.Ala922Thr
XM_011517309.2:c.2764G>A	XP_011515611.1:p.Ala922Thr
XM_011517311.1:c.2332G>A	XP_011515613.1:p.Ala778Thr
XM_011517312.1:c.2293G>A	XP_011515614.1:p.Ala765Thr
XM_011517312.2:c.2293G>A	XP_011515614.1:p.Ala765Thr
XM_017013870.2:c.2764G>A	XP_016869359.1:p.Ala922Thr