Canonical Allele Identifier: CA369957316

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900882C>G (hg19) ; chr8:g.1952716C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952716C>G , CM000670.2:g.1952716C>G	GRCh38
NC_000008.10:g.1900882C>G , CM000670.1:g.1900882C>G	GRCh37
NC_000008.9:g.1888289C>G	NCBI36
NG_008480.1:g.133734C>G , LRG_234:g.133734C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3409C>G MANE Select	ENSP00000340297.3:p.Leu1137Val
ENST00000635773.1:c.3937C>G
ENST00000635855.1:c.*3363C>G	ENSP00000489726.1:n.*3363C>G
ENST00000349830.7:c.3409C>G	ENSP00000340297.3:p.Leu1137Val
ENST00000398564.5:c.3484C>G	ENSP00000381571.1:p.Leu1162Val
ENST00000518288.5:c.3481C>G	ENSP00000431012.1:p.Leu1161Val
ENST00000520359.5:c.3295C>G	ENSP00000427909.1:p.Leu1099Val
ENST00000521927.1:n.246C>G
ENST00000522435.5:c.2341C>G	ENSP00000427768.1:p.Leu781Val
ENST00000523596.5:n.501C>G
NM_001308152.1:c.3295C>G	NP_001295081.1:p.Leu1099Val
NM_001308153.1:c.3481C>G	NP_001295082.1:p.Leu1161Val
NM_014629.2:c.3409C>G , LRG_234t1:c.3409C>G	NP_055444.2:p.Leu1137Val
NM_014629.3:c.3409C>G	NP_055444.2:p.Leu1137Val
XM_005266041.2:c.3412C>G	XP_005266098.1:p.Leu1138Val
XM_011534766.1:c.3325C>G	XP_011533068.1:p.Leu1109Val
XM_011534767.1:c.3292C>G	XP_011533069.1:p.Leu1098Val
XM_011534768.1:c.3401-4033C>G	XP_011533070.1:n.3401-4033C>G
XM_011534769.1:c.3367C>G	XP_011533071.1:p.Leu1123Val
XM_005266041.4:c.3412C>G	XP_005266098.1:p.Leu1138Val
XM_011534767.2:c.3292C>G	XP_011533069.1:p.Leu1098Val
XM_017014003.1:c.3484C>G	XP_016869492.1:p.Leu1162Val
XM_024447334.1:c.3412C>G	XP_024303102.1:p.Leu1138Val
XM_024447335.1:c.3496C>G	XP_024303103.1:p.Leu1166Val
NM_014629.4:c.3409C>G MANE Select	NP_055444.2:p.Leu1137Val
NM_001308152.2:c.3295C>G	NP_001295081.1:p.Leu1099Val
NM_001308153.2:c.3481C>G	NP_001295082.1:p.Leu1161Val