Canonical Allele Identifier: CA369954770
Gene: ARHGEF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1857973A>T , CM000670.2:g.1857973A>T GRCh38
NC_000008.10:g.1806139A>T , CM000670.1:g.1806139A>T GRCh37
NC_000008.9:g.1793546A>T NCBI36
NG_008480.1:g.38991A>T , LRG_234:g.38991A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000349830.8:c.51A>T MANE Select ENSP00000340297.3:p.Lys17Asn
ENST00000635773.1:c.510A>T
ENST00000635855.1:c.*2A>T ENSP00000489726.1:n.*2A>T
ENST00000636175.1:c.441A>T
ENST00000349830.7:c.51A>T ENSP00000340297.3:p.Lys17Asn
ENST00000398564.5:c.123A>T ENSP00000381571.1:p.Lys41Asn
ENST00000518288.5:c.123A>T ENSP00000431012.1:p.Lys41Asn
ENST00000520359.5:c.51A>T ENSP00000427909.1:p.Lys17Asn
NM_001308152.1:c.51A>T NP_001295081.1:p.Lys17Asn
NM_001308153.1:c.123A>T NP_001295082.1:p.Lys41Asn
NM_014629.2:c.51A>T , LRG_234t1:c.51A>T NP_055444.2:p.Lys17Asn
NM_014629.3:c.51A>T NP_055444.2:p.Lys17Asn
XM_005266041.2:c.51A>T XP_005266098.1:p.Lys17Asn
XM_011534766.1:c.51A>T XP_011533068.1:p.Lys17Asn
XM_011534767.1:c.51A>T XP_011533069.1:p.Lys17Asn
XM_011534768.1:c.51A>T XP_011533070.1:p.Lys17Asn
XM_011534769.1:c.6A>T XP_011533071.1:p.Lys2Asn
XM_011534770.1:c.51A>T XP_011533072.1:p.Lys17Asn
XM_005266041.4:c.51A>T XP_005266098.1:p.Lys17Asn
XM_011534767.2:c.51A>T XP_011533069.1:p.Lys17Asn
XM_011534770.2:c.51A>T XP_011533072.1:p.Lys17Asn
XM_017014003.1:c.123A>T XP_016869492.1:p.Lys41Asn
XM_024447334.1:c.51A>T XP_024303102.1:p.Lys17Asn
XM_024447335.1:c.135A>T XP_024303103.1:p.Lys45Asn
NM_014629.4:c.51A>T MANE Select NP_055444.2:p.Lys17Asn
NM_001308152.2:c.51A>T NP_001295081.1:p.Lys17Asn
NM_001308153.2:c.123A>T NP_001295082.1:p.Lys41Asn