Canonical Allele Identifier: CA369957296

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900871G>T (hg19) ; chr8:g.1952705G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952705G>T , CM000670.2:g.1952705G>T	GRCh38
NC_000008.10:g.1900871G>T , CM000670.1:g.1900871G>T	GRCh37
NC_000008.9:g.1888278G>T	NCBI36
NG_008480.1:g.133723G>T , LRG_234:g.133723G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3398G>T MANE Select	ENSP00000340297.3:p.Gly1133Val
ENST00000635773.1:c.3926G>T
ENST00000635855.1:c.*3352G>T	ENSP00000489726.1:n.*3352G>T
ENST00000349830.7:c.3398G>T	ENSP00000340297.3:p.Gly1133Val
ENST00000398564.5:c.3473G>T	ENSP00000381571.1:p.Gly1158Val
ENST00000518288.5:c.3470G>T	ENSP00000431012.1:p.Gly1157Val
ENST00000520359.5:c.3284G>T	ENSP00000427909.1:p.Gly1095Val
ENST00000521927.1:n.235G>T
ENST00000522435.5:c.2330G>T	ENSP00000427768.1:p.Gly777Val
ENST00000523596.5:n.490G>T
NM_001308152.1:c.3284G>T	NP_001295081.1:p.Gly1095Val
NM_001308153.1:c.3470G>T	NP_001295082.1:p.Gly1157Val
NM_014629.2:c.3398G>T , LRG_234t1:c.3398G>T	NP_055444.2:p.Gly1133Val
NM_014629.3:c.3398G>T	NP_055444.2:p.Gly1133Val
XM_005266041.2:c.3401G>T	XP_005266098.1:p.Gly1134Val
XM_011534766.1:c.3314G>T	XP_011533068.1:p.Gly1105Val
XM_011534767.1:c.3281G>T	XP_011533069.1:p.Gly1094Val
XM_011534768.1:c.3401-4044G>T	XP_011533070.1:n.3401-4044G>T
XM_011534769.1:c.3356G>T	XP_011533071.1:p.Gly1119Val
XM_005266041.4:c.3401G>T	XP_005266098.1:p.Gly1134Val
XM_011534767.2:c.3281G>T	XP_011533069.1:p.Gly1094Val
XM_017014003.1:c.3473G>T	XP_016869492.1:p.Gly1158Val
XM_024447334.1:c.3401G>T	XP_024303102.1:p.Gly1134Val
XM_024447335.1:c.3485G>T	XP_024303103.1:p.Gly1162Val
NM_014629.4:c.3398G>T MANE Select	NP_055444.2:p.Gly1133Val
NM_001308152.2:c.3284G>T	NP_001295081.1:p.Gly1095Val
NM_001308153.2:c.3470G>T	NP_001295082.1:p.Gly1157Val