Canonical Allele Identifier: CA4599580

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs756425124
• ExAC: 8:1806176 C / T
• gnomAD v2: 8-1806176-C-T
• MyVariant Identifiers: chr8:g.1806176C>T (hg19) ; chr8:g.1858010C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858010C>T , CM000670.2:g.1858010C>T	GRCh38
NC_000008.10:g.1806176C>T , CM000670.1:g.1806176C>T	GRCh37
NC_000008.9:g.1793583C>T	NCBI36
NG_008480.1:g.39028C>T , LRG_234:g.39028C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.88C>T MANE Select	ENSP00000340297.3:p.Gln30Ter
ENST00000635773.1:c.547C>T
ENST00000635855.1:c.*39C>T	ENSP00000489726.1:n.*39C>T
ENST00000636175.1:c.478C>T
ENST00000349830.7:c.88C>T	ENSP00000340297.3:p.Gln30Ter
ENST00000398564.5:c.160C>T	ENSP00000381571.1:p.Gln54Ter
ENST00000518288.5:c.160C>T	ENSP00000431012.1:p.Gln54Ter
ENST00000520359.5:c.88C>T	ENSP00000427909.1:p.Gln30Ter
NM_001308152.1:c.88C>T	NP_001295081.1:p.Gln30Ter
NM_001308153.1:c.160C>T	NP_001295082.1:p.Gln54Ter
NM_014629.2:c.88C>T , LRG_234t1:c.88C>T	NP_055444.2:p.Gln30Ter
NM_014629.3:c.88C>T	NP_055444.2:p.Gln30Ter
XM_005266041.2:c.88C>T	XP_005266098.1:p.Gln30Ter
XM_011534766.1:c.88C>T	XP_011533068.1:p.Gln30Ter
XM_011534767.1:c.88C>T	XP_011533069.1:p.Gln30Ter
XM_011534768.1:c.88C>T	XP_011533070.1:p.Gln30Ter
XM_011534769.1:c.43C>T	XP_011533071.1:p.Gln15Ter
XM_011534770.1:c.88C>T	XP_011533072.1:p.Gln30Ter
XM_005266041.4:c.88C>T	XP_005266098.1:p.Gln30Ter
XM_011534767.2:c.88C>T	XP_011533069.1:p.Gln30Ter
XM_011534770.2:c.88C>T	XP_011533072.1:p.Gln30Ter
XM_017014003.1:c.160C>T	XP_016869492.1:p.Gln54Ter
XM_024447334.1:c.88C>T	XP_024303102.1:p.Gln30Ter
XM_024447335.1:c.172C>T	XP_024303103.1:p.Gln58Ter
NM_014629.4:c.88C>T MANE Select	NP_055444.2:p.Gln30Ter
NM_001308152.2:c.88C>T	NP_001295081.1:p.Gln30Ter
NM_001308153.2:c.160C>T	NP_001295082.1:p.Gln54Ter