Canonical Allele Identifier: CA2685945852

Gene: ARHGEF10

Linked Data

• gnomAD v4: 8-1858159-C-CCCAGGTGGGTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858166_1858167insGGTCACCAGGTG , CM000670.2:g.1858166_1858167insGGTCACCAGGTG	GRCh38
NC_000008.10:g.1806332_1806333insGGTCACCAGGTG , CM000670.1:g.1806332_1806333insGGTCACCAGGTG	GRCh37
NC_000008.9:g.1793739_1793740insGGTCACCAGGTG	NCBI36
NG_008480.1:g.39184_39185insGGTCACCAGGTG , LRG_234:g.39184_39185insGGTCACCAGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.193+51_193+52insGGTCACCAGGTG MANE Select	ENSP00000340297.3:n.193+51_193+52insGGTCACCAGGTG
ENST00000635773.1:c.652+51_652+52insGGTCACCAGGTG
ENST00000635855.1:c.*144+51_*144+52insGGTCACCAGGTG	ENSP00000489726.1:n.*144+51_*144+52insGGTCACCAGGTG
ENST00000636175.1:c.583+51_583+52insGGTCACCAGGTG
ENST00000349830.7:c.193+51_193+52insGGTCACCAGGTG	ENSP00000340297.3:n.193+51_193+52insGGTCACCAGGTG
ENST00000398564.5:c.265+51_265+52insGGTCACCAGGTG	ENSP00000381571.1:n.265+51_265+52insGGTCACCAGGTG
ENST00000518288.5:c.265+51_265+52insGGTCACCAGGTG	ENSP00000431012.1:n.265+51_265+52insGGTCACCAGGTG
ENST00000520359.5:c.193+51_193+52insGGTCACCAGGTG	ENSP00000427909.1:n.193+51_193+52insGGTCACCAGGTG
NM_001308152.1:c.193+51_193+52insGGTCACCAGGTG	NP_001295081.1:n.193+51_193+52insGGTCACCAGGTG
NM_001308153.1:c.265+51_265+52insGGTCACCAGGTG	NP_001295082.1:n.265+51_265+52insGGTCACCAGGTG
NM_014629.2:c.193+51_193+52insGGTCACCAGGTG , LRG_234t1:c.193+51_193+52insGGTCACCAGGTG	NP_055444.2:n.193+51_193+52insGGTCACCAGGTG
NM_014629.3:c.193+51_193+52insGGTCACCAGGTG	NP_055444.2:n.193+51_193+52insGGTCACCAGGTG
XM_005266041.2:c.193+51_193+52insGGTCACCAGGTG	XP_005266098.1:n.193+51_193+52insGGTCACCAGGTG
XM_011534766.1:c.193+51_193+52insGGTCACCAGGTG	XP_011533068.1:n.193+51_193+52insGGTCACCAGGTG
XM_011534767.1:c.193+51_193+52insGGTCACCAGGTG	XP_011533069.1:n.193+51_193+52insGGTCACCAGGTG
XM_011534768.1:c.193+51_193+52insGGTCACCAGGTG	XP_011533070.1:n.193+51_193+52insGGTCACCAGGTG
XM_011534769.1:c.148+51_148+52insGGTCACCAGGTG	XP_011533071.1:n.148+51_148+52insGGTCACCAGGTG
XM_011534770.1:c.193+51_193+52insGGTCACCAGGTG	XP_011533072.1:n.193+51_193+52insGGTCACCAGGTG
XM_005266041.4:c.193+51_193+52insGGTCACCAGGTG	XP_005266098.1:n.193+51_193+52insGGTCACCAGGTG
XM_011534767.2:c.193+51_193+52insGGTCACCAGGTG	XP_011533069.1:n.193+51_193+52insGGTCACCAGGTG
XM_011534770.2:c.193+51_193+52insGGTCACCAGGTG	XP_011533072.1:n.193+51_193+52insGGTCACCAGGTG
XM_017014003.1:c.265+51_265+52insGGTCACCAGGTG	XP_016869492.1:n.265+51_265+52insGGTCACCAGGTG
XM_024447334.1:c.193+51_193+52insGGTCACCAGGTG	XP_024303102.1:n.193+51_193+52insGGTCACCAGGTG
XM_024447335.1:c.277+51_277+52insGGTCACCAGGTG	XP_024303103.1:n.277+51_277+52insGGTCACCAGGTG
NM_014629.4:c.193+51_193+52insGGTCACCAGGTG MANE Select	NP_055444.2:n.193+51_193+52insGGTCACCAGGTG
NM_001308152.2:c.193+51_193+52insGGTCACCAGGTG	NP_001295081.1:n.193+51_193+52insGGTCACCAGGTG
NM_001308153.2:c.265+51_265+52insGGTCACCAGGTG	NP_001295082.1:n.265+51_265+52insGGTCACCAGGTG