Canonical Allele Identifier: CA156904

Gene: ARHGAP26

Linked Data

• ClinVar Variation Id: 133543
• ClinVar RCV Id: RCV000120056
• dbSNP Id: rs200573018
• ExAC: 5:142513662 C / T
• gnomAD v2: 5-142513662-C-T
• gnomAD v3: 5-143134097-C-T
• gnomAD v4: 5-143134097-C-T
• MyVariant Identifiers: chr5:g.142513662C>T (hg19) ; chr5:g.143134097C>T (hg38)
• PubMed: PMID:24728327

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143134097C>T , CM000667.2:g.143134097C>T	GRCh38
NC_000005.9:g.142513662C>T , CM000667.1:g.142513662C>T	GRCh37
NC_000005.8:g.142493855C>T	NCBI36
NG_016711.1:g.368371C>T
NG_016711.2:g.368728C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274498.9:c.1829C>T	ENSP00000274498.4:p.Thr610Ile
ENST00000642734.1:c.1721C>T	ENSP00000495827.1:p.Thr574Ile
ENST00000645722.2:c.1829C>T MANE Select	ENSP00000495131.1:p.Thr610Ile
ENST00000274498.8:c.1829C>T	ENSP00000274498.4:p.Thr610Ile
ENST00000378004.7:c.1829C>T	ENSP00000367243.3:p.Thr610Ile
ENST00000418236.5:c.544C>T
ENST00000419676.5:c.167C>T	ENSP00000413283.1:p.Thr56Ile
ENST00000424007.1:c.164C>T	ENSP00000400565.1:p.Thr55Ile
ENST00000443674.5:c.685C>T
ENST00000489924.1:n.113C>T
NM_001135608.1:c.1829C>T	NP_001129080.1:p.Thr610Ile
NM_015071.4:c.1829C>T	NP_055886.1:p.Thr610Ile
XM_005268398.3:c.1958C>T	XP_005268455.1:p.Thr653Ile
XM_005268399.3:c.1958C>T	XP_005268456.1:p.Thr653Ile
XM_005268400.3:c.1958C>T	XP_005268457.1:p.Thr653Ile
XM_005268402.3:c.1829C>T	XP_005268459.1:p.Thr610Ile
XM_006714773.2:c.1958C>T	XP_006714836.1:p.Thr653Ile
XR_944311.1:n.2024C>T
XR_944312.1:n.2211C>T
XR_944313.1:n.2019C>T
XR_944314.1:n.2019C>T
XR_944315.1:n.2018C>T
XR_944316.1:n.1877C>T
XR_944317.1:n.2017C>T
XR_944318.1:n.2020C>T
XR_944319.1:n.2015C>T
XR_944320.1:n.2016C>T
XR_944321.1:n.2017C>T
XR_944322.1:n.1164C>T
XR_944323.1:n.842C>T
NM_001135608.2:c.1829C>T	NP_001129080.1:p.Thr610Ile
NM_001349547.1:c.1721C>T	NP_001336476.1:p.Thr574Ile
NM_015071.6:c.1829C>T	NP_055886.1:p.Thr610Ile
NR_146198.1:n.2207C>T
XM_005268398.5:c.1721C>T	XP_005268455.2:p.Thr574Ile
XM_005268399.5:c.1721C>T	XP_005268456.2:p.Thr574Ile
XM_005268402.4:c.1829C>T	XP_005268459.1:p.Thr610Ile
XM_017009247.2:c.1721C>T	XP_016864736.2:p.Thr574Ile
XM_017009248.2:c.1721C>T	XP_016864737.2:p.Thr574Ile
XM_017009249.2:c.1721C>T	XP_016864738.2:p.Thr574Ile
XM_017009250.2:c.1721C>T	XP_016864739.2:p.Thr574Ile
XR_001742044.2:n.1932C>T
XR_001742045.2:n.1866C>T
XR_001742046.2:n.1932C>T
XR_001742047.2:n.1932C>T
XR_001742048.2:n.1932C>T
XR_002956154.1:n.695C>T
XR_002956155.1:n.719C>T
XR_944311.3:n.1932C>T
XR_944312.2:n.2221C>T
XR_944313.3:n.1932C>T
XR_944314.3:n.1932C>T
XR_944315.3:n.1932C>T
XR_944317.3:n.1932C>T
XR_944319.3:n.1932C>T
XR_944320.3:n.1932C>T
XR_944321.3:n.1932C>T
NM_001135608.3:c.1829C>T MANE Select	NP_001129080.1:p.Thr610Ile
NM_001349547.2:c.1721C>T	NP_001336476.1:p.Thr574Ile
NR_146198.2:n.2214C>T