Canonical Allele Identifier: CA170588634

Gene: ARHGEF10

Linked Data

• ClinVar Variation Id: 1229075
• ClinVar RCV Id: RCV001609315
• dbSNP Id: rs35711467
• gnomAD v2: 8-1806041-G-GATCT
• gnomAD v3: 8-1857875-G-GATCT
• gnomAD v4: 8-1857875-G-GATCT
• MyVariant Identifiers: chr8:g.1806044_1806045insTATC (hg19) ; chr8:g.1806045_1806053delinsTATCGATCTATCT (hg19) ; chr8:g.1806045_1806061delinsTATCGATCTATCTATCTATCT (hg19) ; chr8:g.1806041_1806042insATCT (hg19) ; chr8:g.1857878_1857879insTATC (hg38) ; chr8:g.1857879_1857895delinsTATCGATCTATCTATCTATCT (hg38) ; chr8:g.1857875_1857876insATCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857878_1857879insTATC , CM000670.2:g.1857878_1857879insTATC	GRCh38
NC_000008.10:g.1806044_1806045insTATC , CM000670.1:g.1806044_1806045insTATC	GRCh37
NC_000008.9:g.1793451_1793452insTATC	NCBI36
NG_008480.1:g.38896_38897insTATC , LRG_234:g.38896_38897insTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-82_38-81insTATC MANE Select	ENSP00000340297.3:n.38-82_38-81insTATC
ENST00000635773.1:c.497-82_497-81insTATC
ENST00000635855.1:c.628-82_628-81insTATC	ENSP00000489726.1:n.628-82_628-81insTATC
ENST00000636175.1:c.428-82_428-81insTATC
ENST00000349830.7:c.38-82_38-81insTATC	ENSP00000340297.3:n.38-82_38-81insTATC
ENST00000398564.5:c.110-82_110-81insTATC	ENSP00000381571.1:n.110-82_110-81insTATC
ENST00000518288.5:c.110-82_110-81insTATC	ENSP00000431012.1:n.110-82_110-81insTATC
ENST00000520359.5:c.38-82_38-81insTATC	ENSP00000427909.1:n.38-82_38-81insTATC
NM_001308152.1:c.38-82_38-81insTATC	NP_001295081.1:n.38-82_38-81insTATC
NM_001308153.1:c.110-82_110-81insTATC	NP_001295082.1:n.110-82_110-81insTATC
NM_014629.2:c.38-82_38-81insTATC , LRG_234t1:c.38-82_38-81insTATC	NP_055444.2:n.38-82_38-81insTATC
NM_014629.3:c.38-82_38-81insTATC	NP_055444.2:n.38-82_38-81insTATC
XM_005266041.2:c.38-82_38-81insTATC	XP_005266098.1:n.38-82_38-81insTATC
XM_011534766.1:c.38-82_38-81insTATC	XP_011533068.1:n.38-82_38-81insTATC
XM_011534767.1:c.38-82_38-81insTATC	XP_011533069.1:n.38-82_38-81insTATC
XM_011534768.1:c.38-82_38-81insTATC	XP_011533070.1:n.38-82_38-81insTATC
XM_011534769.1:c.-8-82_-8-81insTATC	XP_011533071.1:n.-8-82_-8-81insTATC
XM_011534770.1:c.38-82_38-81insTATC	XP_011533072.1:n.38-82_38-81insTATC
XM_005266041.4:c.38-82_38-81insTATC	XP_005266098.1:n.38-82_38-81insTATC
XM_011534767.2:c.38-82_38-81insTATC	XP_011533069.1:n.38-82_38-81insTATC
XM_011534770.2:c.38-82_38-81insTATC	XP_011533072.1:n.38-82_38-81insTATC
XM_017014003.1:c.110-82_110-81insTATC	XP_016869492.1:n.110-82_110-81insTATC
XM_024447334.1:c.38-82_38-81insTATC	XP_024303102.1:n.38-82_38-81insTATC
XM_024447335.1:c.122-82_122-81insTATC	XP_024303103.1:n.122-82_122-81insTATC
NM_014629.4:c.38-82_38-81insTATC MANE Select	NP_055444.2:n.38-82_38-81insTATC
NM_001308152.2:c.38-82_38-81insTATC	NP_001295081.1:n.38-82_38-81insTATC
NM_001308153.2:c.110-82_110-81insTATC	NP_001295082.1:n.110-82_110-81insTATC