Canonical Allele Identifier: CA2685945621
Gene: ARHGEF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1857873_1857874insTGAT , CM000670.2:g.1857873_1857874insTGAT GRCh38
NC_000008.10:g.1806039_1806040insTGAT , CM000670.1:g.1806039_1806040insTGAT GRCh37
NC_000008.9:g.1793446_1793447insTGAT NCBI36
NG_008480.1:g.38891_38892insTGAT , LRG_234:g.38891_38892insTGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000349830.8:c.38-87_38-86insTGAT MANE Select ENSP00000340297.3:n.38-87_38-86insTGAT
ENST00000635773.1:c.497-87_497-86insTGAT
ENST00000635855.1:c.628-87_628-86insTGAT ENSP00000489726.1:n.628-87_628-86insTGAT
ENST00000636175.1:c.428-87_428-86insTGAT
ENST00000349830.7:c.38-87_38-86insTGAT ENSP00000340297.3:n.38-87_38-86insTGAT
ENST00000398564.5:c.110-87_110-86insTGAT ENSP00000381571.1:n.110-87_110-86insTGAT
ENST00000518288.5:c.110-87_110-86insTGAT ENSP00000431012.1:n.110-87_110-86insTGAT
ENST00000520359.5:c.38-87_38-86insTGAT ENSP00000427909.1:n.38-87_38-86insTGAT
NM_001308152.1:c.38-87_38-86insTGAT NP_001295081.1:n.38-87_38-86insTGAT
NM_001308153.1:c.110-87_110-86insTGAT NP_001295082.1:n.110-87_110-86insTGAT
NM_014629.2:c.38-87_38-86insTGAT , LRG_234t1:c.38-87_38-86insTGAT NP_055444.2:n.38-87_38-86insTGAT
NM_014629.3:c.38-87_38-86insTGAT NP_055444.2:n.38-87_38-86insTGAT
XM_005266041.2:c.38-87_38-86insTGAT XP_005266098.1:n.38-87_38-86insTGAT
XM_011534766.1:c.38-87_38-86insTGAT XP_011533068.1:n.38-87_38-86insTGAT
XM_011534767.1:c.38-87_38-86insTGAT XP_011533069.1:n.38-87_38-86insTGAT
XM_011534768.1:c.38-87_38-86insTGAT XP_011533070.1:n.38-87_38-86insTGAT
XM_011534769.1:c.-8-87_-8-86insTGAT XP_011533071.1:n.-8-87_-8-86insTGAT
XM_011534770.1:c.38-87_38-86insTGAT XP_011533072.1:n.38-87_38-86insTGAT
XM_005266041.4:c.38-87_38-86insTGAT XP_005266098.1:n.38-87_38-86insTGAT
XM_011534767.2:c.38-87_38-86insTGAT XP_011533069.1:n.38-87_38-86insTGAT
XM_011534770.2:c.38-87_38-86insTGAT XP_011533072.1:n.38-87_38-86insTGAT
XM_017014003.1:c.110-87_110-86insTGAT XP_016869492.1:n.110-87_110-86insTGAT
XM_024447334.1:c.38-87_38-86insTGAT XP_024303102.1:n.38-87_38-86insTGAT
XM_024447335.1:c.122-87_122-86insTGAT XP_024303103.1:n.122-87_122-86insTGAT
NM_014629.4:c.38-87_38-86insTGAT MANE Select NP_055444.2:n.38-87_38-86insTGAT
NM_001308152.2:c.38-87_38-86insTGAT NP_001295081.1:n.38-87_38-86insTGAT
NM_001308153.2:c.110-87_110-86insTGAT NP_001295082.1:n.110-87_110-86insTGAT