Canonical Allele Identifier: CA369967573

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1928457A>G , CM000670.2:g.1928457A>G	GRCh38
NC_000008.10:g.1876623A>G , CM000670.1:g.1876623A>G	GRCh37
NC_000008.9:g.1864030A>G	NCBI36
NG_008480.1:g.109475A>G , LRG_234:g.109475A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.2728A>G MANE Select	ENSP00000340297.3:p.Ile910Val
ENST00000635773.1:c.3256A>G
ENST00000635855.1:c.*2682A>G	ENSP00000489726.1:n.*2682A>G
ENST00000349830.7:c.2728A>G	ENSP00000340297.3:p.Ile910Val
ENST00000398564.5:c.2803A>G	ENSP00000381571.1:p.Ile935Val
ENST00000518288.5:c.2800A>G	ENSP00000431012.1:p.Ile934Val
ENST00000520359.5:c.2614A>G	ENSP00000427909.1:p.Ile872Val
ENST00000522435.5:c.1660A>G	ENSP00000427768.1:p.Ile554Val
NM_001308152.1:c.2614A>G	NP_001295081.1:p.Ile872Val
NM_001308153.1:c.2800A>G	NP_001295082.1:p.Ile934Val
NM_014629.2:c.2728A>G , LRG_234t1:c.2728A>G	NP_055444.2:p.Ile910Val
NM_014629.3:c.2728A>G	NP_055444.2:p.Ile910Val
XM_005266041.2:c.2731A>G	XP_005266098.1:p.Ile911Val
XM_011534766.1:c.2644A>G	XP_011533068.1:p.Ile882Val
XM_011534767.1:c.2611A>G	XP_011533069.1:p.Ile871Val
XM_011534768.1:c.2731A>G	XP_011533070.1:p.Ile911Val
XM_011534769.1:c.2686A>G	XP_011533071.1:p.Ile896Val
XM_011534770.1:c.2731A>G	XP_011533072.1:p.Ile911Val
XM_005266041.4:c.2731A>G	XP_005266098.1:p.Ile911Val
XM_011534767.2:c.2611A>G	XP_011533069.1:p.Ile871Val
XM_011534770.2:c.2731A>G	XP_011533072.1:p.Ile911Val
XM_017014003.1:c.2803A>G	XP_016869492.1:p.Ile935Val
XM_024447334.1:c.2731A>G	XP_024303102.1:p.Ile911Val
XM_024447335.1:c.2815A>G	XP_024303103.1:p.Ile939Val
NM_014629.4:c.2728A>G MANE Select	NP_055444.2:p.Ile910Val
NM_001308152.2:c.2614A>G	NP_001295081.1:p.Ile872Val
NM_001308153.2:c.2800A>G	NP_001295082.1:p.Ile934Val