Canonical Allele Identifier: CA1757784827

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952491_1952492delinsAG , CM000670.2:g.1952491_1952492delinsAG	GRCh38
NC_000008.10:g.1900657_1900658delinsAG , CM000670.1:g.1900657_1900658delinsAG	GRCh37
NC_000008.9:g.1888064_1888065delinsAG	NCBI36
NG_008480.1:g.133509_133510delinsAG , LRG_234:g.133509_133510delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.3398-214_3398-213delinsAG MANE Select	ENSP00000340297.3:n.3398-214_3398-213delinsAG
ENST00000635773.1:c.3926-214_3926-213delinsAG
ENST00000635855.1:c.*3352-214_*3352-213delinsAG	ENSP00000489726.1:n.*3352-214_*3352-213delinsAG
ENST00000349830.7:c.3398-214_3398-213delinsAG	ENSP00000340297.3:n.3398-214_3398-213delinsAG
ENST00000398564.5:c.3473-214_3473-213delinsAG	ENSP00000381571.1:n.3473-214_3473-213delinsAG
ENST00000518288.5:c.3470-214_3470-213delinsAG	ENSP00000431012.1:n.3470-214_3470-213delinsAG
ENST00000520359.5:c.3284-214_3284-213delinsAG	ENSP00000427909.1:n.3284-214_3284-213delinsAG
ENST00000521927.1:n.235-214_235-213delinsAG
ENST00000522435.5:c.2330-214_2330-213delinsAG	ENSP00000427768.1:n.2330-214_2330-213delinsAG
ENST00000523596.5:n.490-214_490-213delinsAG
NM_001308152.1:c.3284-214_3284-213delinsAG	NP_001295081.1:n.3284-214_3284-213delinsAG
NM_001308153.1:c.3470-214_3470-213delinsAG	NP_001295082.1:n.3470-214_3470-213delinsAG
NM_014629.2:c.3398-214_3398-213delinsAG , LRG_234t1:c.3398-214_3398-213delinsAG	NP_055444.2:n.3398-214_3398-213delinsAG
NM_014629.3:c.3398-214_3398-213delinsAG	NP_055444.2:n.3398-214_3398-213delinsAG
XM_005266041.2:c.3401-214_3401-213delinsAG	XP_005266098.1:n.3401-214_3401-213delinsAG
XM_011534766.1:c.3314-214_3314-213delinsAG	XP_011533068.1:n.3314-214_3314-213delinsAG
XM_011534767.1:c.3281-214_3281-213delinsAG	XP_011533069.1:n.3281-214_3281-213delinsAG
XM_011534768.1:c.3401-4258_3401-4257delinsAG	XP_011533070.1:n.3401-4258_3401-4257delinsAG
XM_011534769.1:c.3356-214_3356-213delinsAG	XP_011533071.1:n.3356-214_3356-213delinsAG
XM_005266041.4:c.3401-214_3401-213delinsAG	XP_005266098.1:n.3401-214_3401-213delinsAG
XM_011534767.2:c.3281-214_3281-213delinsAG	XP_011533069.1:n.3281-214_3281-213delinsAG
XM_017014003.1:c.3473-214_3473-213delinsAG	XP_016869492.1:n.3473-214_3473-213delinsAG
XM_024447334.1:c.3401-214_3401-213delinsAG	XP_024303102.1:n.3401-214_3401-213delinsAG
XM_024447335.1:c.3485-214_3485-213delinsAG	XP_024303103.1:n.3485-214_3485-213delinsAG
NM_014629.4:c.3398-214_3398-213delinsAG MANE Select	NP_055444.2:n.3398-214_3398-213delinsAG
NM_001308152.2:c.3284-214_3284-213delinsAG	NP_001295081.1:n.3284-214_3284-213delinsAG
NM_001308153.2:c.3470-214_3470-213delinsAG	NP_001295082.1:n.3470-214_3470-213delinsAG