Canonical Allele Identifier: CA369957293

Gene: ARHGEF10

Linked Data

• COSMIC: COSM4662995 ; COSM4662996
• MyVariant Identifiers: chr8:g.1900870G>T (hg19) ; chr8:g.1952704G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952704G>T , CM000670.2:g.1952704G>T	GRCh38
NC_000008.10:g.1900870G>T , CM000670.1:g.1900870G>T	GRCh37
NC_000008.9:g.1888277G>T	NCBI36
NG_008480.1:g.133722G>T , LRG_234:g.133722G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3398-1G>T MANE Select	ENSP00000340297.3:n.3398-1G>T
ENST00000635773.1:c.3926-1G>T
ENST00000635855.1:c.*3352-1G>T	ENSP00000489726.1:n.*3352-1G>T
ENST00000349830.7:c.3398-1G>T	ENSP00000340297.3:n.3398-1G>T
ENST00000398564.5:c.3473-1G>T	ENSP00000381571.1:n.3473-1G>T
ENST00000518288.5:c.3470-1G>T	ENSP00000431012.1:n.3470-1G>T
ENST00000520359.5:c.3284-1G>T	ENSP00000427909.1:n.3284-1G>T
ENST00000521927.1:n.235-1G>T
ENST00000522435.5:c.2330-1G>T	ENSP00000427768.1:n.2330-1G>T
ENST00000523596.5:n.490-1G>T
NM_001308152.1:c.3284-1G>T	NP_001295081.1:n.3284-1G>T
NM_001308153.1:c.3470-1G>T	NP_001295082.1:n.3470-1G>T
NM_014629.2:c.3398-1G>T , LRG_234t1:c.3398-1G>T	NP_055444.2:n.3398-1G>T
NM_014629.3:c.3398-1G>T	NP_055444.2:n.3398-1G>T
XM_005266041.2:c.3401-1G>T	XP_005266098.1:n.3401-1G>T
XM_011534766.1:c.3314-1G>T	XP_011533068.1:n.3314-1G>T
XM_011534767.1:c.3281-1G>T	XP_011533069.1:n.3281-1G>T
XM_011534768.1:c.3401-4045G>T	XP_011533070.1:n.3401-4045G>T
XM_011534769.1:c.3356-1G>T	XP_011533071.1:n.3356-1G>T
XM_005266041.4:c.3401-1G>T	XP_005266098.1:n.3401-1G>T
XM_011534767.2:c.3281-1G>T	XP_011533069.1:n.3281-1G>T
XM_017014003.1:c.3473-1G>T	XP_016869492.1:n.3473-1G>T
XM_024447334.1:c.3401-1G>T	XP_024303102.1:n.3401-1G>T
XM_024447335.1:c.3485-1G>T	XP_024303103.1:n.3485-1G>T
NM_014629.4:c.3398-1G>T MANE Select	NP_055444.2:n.3398-1G>T
NM_001308152.2:c.3284-1G>T	NP_001295081.1:n.3284-1G>T
NM_001308153.2:c.3470-1G>T	NP_001295082.1:n.3470-1G>T