Canonical Allele Identifier: CA459050208

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1815155521
• gnomAD v4: 8-1952716-C-T
• MyVariant Identifiers: chr8:g.1900882C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.3409C>T MANE Select	ENSP00000340297.3:p.Leu1137=
ENST00000635773.1:c.3937C>T
ENST00000635855.1:c.*3363C>T	ENSP00000489726.1:n.*3363C>T
ENST00000349830.7:c.3409C>T	ENSP00000340297.3:p.Leu1137=
ENST00000398564.5:c.3484C>T	ENSP00000381571.1:p.Leu1162=
ENST00000518288.5:c.3481C>T	ENSP00000431012.1:p.Leu1161=
ENST00000520359.5:c.3295C>T	ENSP00000427909.1:p.Leu1099=
ENST00000521927.1:n.246C>T
ENST00000522435.5:c.2341C>T	ENSP00000427768.1:p.Leu781=
ENST00000523596.5:n.501C>T
NM_001308152.1:c.3295C>T	NP_001295081.1:p.Leu1099=
NM_001308153.1:c.3481C>T	NP_001295082.1:p.Leu1161=
NM_014629.2:c.3409C>T , LRG_234t1:c.3409C>T	NP_055444.2:p.Leu1137=
NM_014629.3:c.3409C>T	NP_055444.2:p.Leu1137=
XM_005266041.2:c.3412C>T	XP_005266098.1:p.Leu1138=
XM_011534766.1:c.3325C>T	XP_011533068.1:p.Leu1109=
XM_011534767.1:c.3292C>T	XP_011533069.1:p.Leu1098=
XM_011534768.1:c.3401-4033C>T	XP_011533070.1:n.3401-4033C>T
XM_011534769.1:c.3367C>T	XP_011533071.1:p.Leu1123=
XM_005266041.4:c.3412C>T	XP_005266098.1:p.Leu1138=
XM_011534767.2:c.3292C>T	XP_011533069.1:p.Leu1098=
XM_017014003.1:c.3484C>T	XP_016869492.1:p.Leu1162=
XM_024447334.1:c.3412C>T	XP_024303102.1:p.Leu1138=
XM_024447335.1:c.3496C>T	XP_024303103.1:p.Leu1166=
NM_014629.4:c.3409C>T MANE Select	NP_055444.2:p.Leu1137=
NM_001308152.2:c.3295C>T	NP_001295081.1:p.Leu1099=
NM_001308153.2:c.3481C>T	NP_001295082.1:p.Leu1161=