Canonical Allele Identifier: CA4599662
Gene: ARHGEF10 HGNC NCBI

Linked Data

dbSNP Id: rs772027392
gnomAD v2: 8-1806331-T-TG
gnomAD v3: 8-1858165-T-TG
gnomAD v4: 8-1858165-T-TG

Genomic Alleles

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

Transcript Alleles

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