Canonical Allele Identifier: CA4599638

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1554478157
• ExAC: 8:1806309 A / AGTCCCCAGGAGGGTCCCCAGGTGG
• gnomAD v3: 8-1858143-A-AGTCCCCAGGAGGGTCCCCAGGTGG
• gnomAD v4: 8-1858143-A-AGTCCCCAGGAGGGTCCCCAGGTGG
• MyVariant Identifiers: chr8:g.1806309_1806310insGTCCCCAGGAGGGTCCCCAGGTGG (hg19) ; chr8:g.1858143_1858144insGTCCCCAGGAGGGTCCCCAGGTGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858152_1858153insAGGGTCCCCAGGTGGGTCCCCAGG , CM000670.2:g.1858152_1858153insAGGGTCCCCAGGTGGGTCCCCAGG	GRCh38
NC_000008.10:g.1806318_1806319insAGGGTCCCCAGGTGGGTCCCCAGG , CM000670.1:g.1806318_1806319insAGGGTCCCCAGGTGGGTCCCCAGG	GRCh37
NC_000008.9:g.1793725_1793726insAGGGTCCCCAGGTGGGTCCCCAGG	NCBI36
NG_008480.1:g.39170_39171insAGGGTCCCCAGGTGGGTCCCCAGG , LRG_234:g.39170_39171insAGGGTCCCCAGGTGGGTCCCCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG MANE Select	ENSP00000340297.3:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
ENST00000635773.1:c.652+37_652+38insAGGGTCCCCAGGTGGGTCCCCAGG
ENST00000635855.1:c.*144+37_*144+38insAGGGTCCCCAGGTGGGTCCCCAGG	ENSP00000489726.1:n.*144+37_*144+38insAGGGTCCCCAGGTGGGTCCCCAG...
ENST00000636175.1:c.583+37_583+38insAGGGTCCCCAGGTGGGTCCCCAGG
ENST00000349830.7:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	ENSP00000340297.3:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
ENST00000398564.5:c.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG	ENSP00000381571.1:n.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG
ENST00000518288.5:c.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG	ENSP00000431012.1:n.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG
ENST00000520359.5:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	ENSP00000427909.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
NM_001308152.1:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	NP_001295081.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
NM_001308153.1:c.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG	NP_001295082.1:n.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG
NM_014629.2:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG , LRG_234t1:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	NP_055444.2:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
NM_014629.3:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	NP_055444.2:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_005266041.2:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_005266098.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_011534766.1:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_011533068.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_011534767.1:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_011533069.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_011534768.1:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_011533070.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_011534769.1:c.148+37_148+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_011533071.1:n.148+37_148+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_011534770.1:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_011533072.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_005266041.4:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_005266098.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_011534767.2:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_011533069.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_011534770.2:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_011533072.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_017014003.1:c.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_016869492.1:n.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_024447334.1:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_024303102.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
XM_024447335.1:c.277+37_277+38insAGGGTCCCCAGGTGGGTCCCCAGG	XP_024303103.1:n.277+37_277+38insAGGGTCCCCAGGTGGGTCCCCAGG
NM_014629.4:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG MANE Select	NP_055444.2:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
NM_001308152.2:c.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG	NP_001295081.1:n.193+37_193+38insAGGGTCCCCAGGTGGGTCCCCAGG
NM_001308153.2:c.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG	NP_001295082.1:n.265+37_265+38insAGGGTCCCCAGGTGGGTCCCCAGG