Canonical Allele Identifier: CA369954962

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1806228C>T (hg19) ; chr8:g.1858062C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858062C>T , CM000670.2:g.1858062C>T	GRCh38
NC_000008.10:g.1806228C>T , CM000670.1:g.1806228C>T	GRCh37
NC_000008.9:g.1793635C>T	NCBI36
NG_008480.1:g.39080C>T , LRG_234:g.39080C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.140C>T MANE Select	ENSP00000340297.3:p.Pro47Leu
ENST00000635773.1:c.599C>T
ENST00000635855.1:c.*91C>T	ENSP00000489726.1:n.*91C>T
ENST00000636175.1:c.530C>T
ENST00000349830.7:c.140C>T	ENSP00000340297.3:p.Pro47Leu
ENST00000398564.5:c.212C>T	ENSP00000381571.1:p.Pro71Leu
ENST00000518288.5:c.212C>T	ENSP00000431012.1:p.Pro71Leu
ENST00000520359.5:c.140C>T	ENSP00000427909.1:p.Pro47Leu
NM_001308152.1:c.140C>T	NP_001295081.1:p.Pro47Leu
NM_001308153.1:c.212C>T	NP_001295082.1:p.Pro71Leu
NM_014629.2:c.140C>T , LRG_234t1:c.140C>T	NP_055444.2:p.Pro47Leu
NM_014629.3:c.140C>T	NP_055444.2:p.Pro47Leu
XM_005266041.2:c.140C>T	XP_005266098.1:p.Pro47Leu
XM_011534766.1:c.140C>T	XP_011533068.1:p.Pro47Leu
XM_011534767.1:c.140C>T	XP_011533069.1:p.Pro47Leu
XM_011534768.1:c.140C>T	XP_011533070.1:p.Pro47Leu
XM_011534769.1:c.95C>T	XP_011533071.1:p.Pro32Leu
XM_011534770.1:c.140C>T	XP_011533072.1:p.Pro47Leu
XM_005266041.4:c.140C>T	XP_005266098.1:p.Pro47Leu
XM_011534767.2:c.140C>T	XP_011533069.1:p.Pro47Leu
XM_011534770.2:c.140C>T	XP_011533072.1:p.Pro47Leu
XM_017014003.1:c.212C>T	XP_016869492.1:p.Pro71Leu
XM_024447334.1:c.140C>T	XP_024303102.1:p.Pro47Leu
XM_024447335.1:c.224C>T	XP_024303103.1:p.Pro75Leu
NM_014629.4:c.140C>T MANE Select	NP_055444.2:p.Pro47Leu
NM_001308152.2:c.140C>T	NP_001295081.1:p.Pro47Leu
NM_001308153.2:c.212C>T	NP_001295082.1:p.Pro71Leu