Canonical Allele Identifier: CA1757784837

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1815136547

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952494T>G , CM000670.2:g.1952494T>G	GRCh38
NC_000008.10:g.1900660T>G , CM000670.1:g.1900660T>G	GRCh37
NC_000008.9:g.1888067T>G	NCBI36
NG_008480.1:g.133512T>G , LRG_234:g.133512T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.3398-211T>G MANE Select	ENSP00000340297.3:n.3398-211T>G
ENST00000635773.1:c.3926-211T>G
ENST00000635855.1:c.*3352-211T>G	ENSP00000489726.1:n.*3352-211T>G
ENST00000349830.7:c.3398-211T>G	ENSP00000340297.3:n.3398-211T>G
ENST00000398564.5:c.3473-211T>G	ENSP00000381571.1:n.3473-211T>G
ENST00000518288.5:c.3470-211T>G	ENSP00000431012.1:n.3470-211T>G
ENST00000520359.5:c.3284-211T>G	ENSP00000427909.1:n.3284-211T>G
ENST00000521927.1:n.235-211T>G
ENST00000522435.5:c.2330-211T>G	ENSP00000427768.1:n.2330-211T>G
ENST00000523596.5:n.490-211T>G
NM_001308152.1:c.3284-211T>G	NP_001295081.1:n.3284-211T>G
NM_001308153.1:c.3470-211T>G	NP_001295082.1:n.3470-211T>G
NM_014629.2:c.3398-211T>G , LRG_234t1:c.3398-211T>G	NP_055444.2:n.3398-211T>G
NM_014629.3:c.3398-211T>G	NP_055444.2:n.3398-211T>G
XM_005266041.2:c.3401-211T>G	XP_005266098.1:n.3401-211T>G
XM_011534766.1:c.3314-211T>G	XP_011533068.1:n.3314-211T>G
XM_011534767.1:c.3281-211T>G	XP_011533069.1:n.3281-211T>G
XM_011534768.1:c.3401-4255T>G	XP_011533070.1:n.3401-4255T>G
XM_011534769.1:c.3356-211T>G	XP_011533071.1:n.3356-211T>G
XM_005266041.4:c.3401-211T>G	XP_005266098.1:n.3401-211T>G
XM_011534767.2:c.3281-211T>G	XP_011533069.1:n.3281-211T>G
XM_017014003.1:c.3473-211T>G	XP_016869492.1:n.3473-211T>G
XM_024447334.1:c.3401-211T>G	XP_024303102.1:n.3401-211T>G
XM_024447335.1:c.3485-211T>G	XP_024303103.1:n.3485-211T>G
NM_014629.4:c.3398-211T>G MANE Select	NP_055444.2:n.3398-211T>G
NM_001308152.2:c.3284-211T>G	NP_001295081.1:n.3284-211T>G
NM_001308153.2:c.3470-211T>G	NP_001295082.1:n.3470-211T>G