Canonical Allele Identifier: CA1109656661

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1805687787
• gnomAD v3: 8-1857890-CT-C
• gnomAD v4: 8-1857890-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857891del , CM000670.2:g.1857891del	GRCh38
NC_000008.10:g.1806057del , CM000670.1:g.1806057del	GRCh37
NC_000008.9:g.1793464del	NCBI36
NG_008480.1:g.38909del , LRG_234:g.38909del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-69del MANE Select	ENSP00000340297.3:n.38-69del
ENST00000635773.1:c.497-69del
ENST00000635855.1:c.628-69del	ENSP00000489726.1:n.628-69del
ENST00000636175.1:c.428-69del
ENST00000349830.7:c.38-69del	ENSP00000340297.3:n.38-69del
ENST00000398564.5:c.110-69del	ENSP00000381571.1:n.110-69del
ENST00000518288.5:c.110-69del	ENSP00000431012.1:n.110-69del
ENST00000520359.5:c.38-69del	ENSP00000427909.1:n.38-69del
NM_001308152.1:c.38-69del	NP_001295081.1:n.38-69del
NM_001308153.1:c.110-69del	NP_001295082.1:n.110-69del
NM_014629.2:c.38-69del , LRG_234t1:c.38-69del	NP_055444.2:n.38-69del
NM_014629.3:c.38-69del	NP_055444.2:n.38-69del
XM_005266041.2:c.38-69del	XP_005266098.1:n.38-69del
XM_011534766.1:c.38-69del	XP_011533068.1:n.38-69del
XM_011534767.1:c.38-69del	XP_011533069.1:n.38-69del
XM_011534768.1:c.38-69del	XP_011533070.1:n.38-69del
XM_011534769.1:c.-8-69del	XP_011533071.1:n.-8-69del
XM_011534770.1:c.38-69del	XP_011533072.1:n.38-69del
XM_005266041.4:c.38-69del	XP_005266098.1:n.38-69del
XM_011534767.2:c.38-69del	XP_011533069.1:n.38-69del
XM_011534770.2:c.38-69del	XP_011533072.1:n.38-69del
XM_017014003.1:c.110-69del	XP_016869492.1:n.110-69del
XM_024447334.1:c.38-69del	XP_024303102.1:n.38-69del
XM_024447335.1:c.122-69del	XP_024303103.1:n.122-69del
NM_014629.4:c.38-69del MANE Select	NP_055444.2:n.38-69del
NM_001308152.2:c.38-69del	NP_001295081.1:n.38-69del
NM_001308153.2:c.110-69del	NP_001295082.1:n.110-69del