Canonical Allele Identifier: CA459054514

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1806238T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858072T>C , CM000670.2:g.1858072T>C	GRCh38
NC_000008.10:g.1806238T>C , CM000670.1:g.1806238T>C	GRCh37
NC_000008.9:g.1793645T>C	NCBI36
NG_008480.1:g.39090T>C , LRG_234:g.39090T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.150T>C MANE Select	ENSP00000340297.3:p.Pro50=
ENST00000635773.1:c.609T>C
ENST00000635855.1:c.*101T>C	ENSP00000489726.1:n.*101T>C
ENST00000636175.1:c.540T>C
ENST00000349830.7:c.150T>C	ENSP00000340297.3:p.Pro50=
ENST00000398564.5:c.222T>C	ENSP00000381571.1:p.Pro74=
ENST00000518288.5:c.222T>C	ENSP00000431012.1:p.Pro74=
ENST00000520359.5:c.150T>C	ENSP00000427909.1:p.Pro50=
NM_001308152.1:c.150T>C	NP_001295081.1:p.Pro50=
NM_001308153.1:c.222T>C	NP_001295082.1:p.Pro74=
NM_014629.2:c.150T>C , LRG_234t1:c.150T>C	NP_055444.2:p.Pro50=
NM_014629.3:c.150T>C	NP_055444.2:p.Pro50=
XM_005266041.2:c.150T>C	XP_005266098.1:p.Pro50=
XM_011534766.1:c.150T>C	XP_011533068.1:p.Pro50=
XM_011534767.1:c.150T>C	XP_011533069.1:p.Pro50=
XM_011534768.1:c.150T>C	XP_011533070.1:p.Pro50=
XM_011534769.1:c.105T>C	XP_011533071.1:p.Pro35=
XM_011534770.1:c.150T>C	XP_011533072.1:p.Pro50=
XM_005266041.4:c.150T>C	XP_005266098.1:p.Pro50=
XM_011534767.2:c.150T>C	XP_011533069.1:p.Pro50=
XM_011534770.2:c.150T>C	XP_011533072.1:p.Pro50=
XM_017014003.1:c.222T>C	XP_016869492.1:p.Pro74=
XM_024447334.1:c.150T>C	XP_024303102.1:p.Pro50=
XM_024447335.1:c.234T>C	XP_024303103.1:p.Pro78=
NM_014629.4:c.150T>C MANE Select	NP_055444.2:p.Pro50=
NM_001308152.2:c.150T>C	NP_001295081.1:p.Pro50=
NM_001308153.2:c.222T>C	NP_001295082.1:p.Pro74=