Canonical Allele Identifier: CA1109657497

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1805737784
• gnomAD v3: 8-1858155-GGTCCCCAGGTGAGTCCCCAGGTGGGTCCCCATGTGAGTCACCAGGTGAGTTCCCAGGTGAGTCCCCAGGTGA-G
• gnomAD v4: 8-1858155-GGTCCCCAGGTGAGTCCCCAGGTGGGTCCCCATGTGAGTCACCAGGTGAGTTCCCAGGTGAGTCCCCAGGTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858167_1858238del , CM000670.2:g.1858167_1858238del	GRCh38
NC_000008.10:g.1806333_1806404del , CM000670.1:g.1806333_1806404del	GRCh37
NC_000008.9:g.1793740_1793811del	NCBI36
NG_008480.1:g.39185_39256del , LRG_234:g.39185_39256del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.193+52_193+123del MANE Select	ENSP00000340297.3:n.193+52_193+123del
ENST00000635773.1:c.652+52_652+123del
ENST00000635855.1:c.*144+52_*144+123del	ENSP00000489726.1:n.*144+52_*144+123del
ENST00000636175.1:c.583+52_583+123del
ENST00000349830.7:c.193+52_193+123del	ENSP00000340297.3:n.193+52_193+123del
ENST00000398564.5:c.265+52_265+123del	ENSP00000381571.1:n.265+52_265+123del
ENST00000518288.5:c.265+52_265+123del	ENSP00000431012.1:n.265+52_265+123del
ENST00000520359.5:c.193+52_193+123del	ENSP00000427909.1:n.193+52_193+123del
NM_001308152.1:c.193+52_193+123del	NP_001295081.1:n.193+52_193+123del
NM_001308153.1:c.265+52_265+123del	NP_001295082.1:n.265+52_265+123del
NM_014629.2:c.193+52_193+123del , LRG_234t1:c.193+52_193+123del	NP_055444.2:n.193+52_193+123del
NM_014629.3:c.193+52_193+123del	NP_055444.2:n.193+52_193+123del
XM_005266041.2:c.193+52_193+123del	XP_005266098.1:n.193+52_193+123del
XM_011534766.1:c.193+52_193+123del	XP_011533068.1:n.193+52_193+123del
XM_011534767.1:c.193+52_193+123del	XP_011533069.1:n.193+52_193+123del
XM_011534768.1:c.193+52_193+123del	XP_011533070.1:n.193+52_193+123del
XM_011534769.1:c.148+52_148+123del	XP_011533071.1:n.148+52_148+123del
XM_011534770.1:c.193+52_193+123del	XP_011533072.1:n.193+52_193+123del
XM_005266041.4:c.193+52_193+123del	XP_005266098.1:n.193+52_193+123del
XM_011534767.2:c.193+52_193+123del	XP_011533069.1:n.193+52_193+123del
XM_011534770.2:c.193+52_193+123del	XP_011533072.1:n.193+52_193+123del
XM_017014003.1:c.265+52_265+123del	XP_016869492.1:n.265+52_265+123del
XM_024447334.1:c.193+52_193+123del	XP_024303102.1:n.193+52_193+123del
XM_024447335.1:c.277+52_277+123del	XP_024303103.1:n.277+52_277+123del
NM_014629.4:c.193+52_193+123del MANE Select	NP_055444.2:n.193+52_193+123del
NM_001308152.2:c.193+52_193+123del	NP_001295081.1:n.193+52_193+123del
NM_001308153.2:c.265+52_265+123del	NP_001295082.1:n.265+52_265+123del