Canonical Allele Identifier: CA383256908

Gene: ARHGAP32

Linked Data

• ClinVar Variation Id: 487793
• ClinVar RCV Id: RCV000577845
• dbSNP Id: rs749174548
• MyVariant Identifiers: chr11:g.128840363G>C (hg19) ; chr11:g.128970468G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128970468G>C , CM000673.2:g.128970468G>C	GRCh38
NC_000011.9:g.128840363G>C , CM000673.1:g.128840363G>C	GRCh37
NC_000011.8:g.128345573G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682385.1:c.4745C>G MANE Select	ENSP00000507720.1:p.Thr1582Ser
ENST00000310343.13:c.4703C>G	ENSP00000310561.8:p.Thr1568Ser
ENST00000392657.7:c.3656C>G	ENSP00000376425.3:p.Thr1219Ser
ENST00000524655.5:c.*3624C>G	ENSP00000432468.1:n.*3624C>G
ENST00000526162.5:n.4325C>G
ENST00000527272.1:c.3656C>G	ENSP00000432862.1:p.Thr1219Ser
NM_001142685.1:c.4703C>G	NP_001136157.1:p.Thr1568Ser
NM_014715.3:c.3656C>G	NP_055530.2:p.Thr1219Ser
XM_005271736.3:c.4745C>G	XP_005271793.2:p.Thr1582Ser
XM_011543072.1:c.4625C>G	XP_011541374.1:p.Thr1542Ser
XM_011543073.1:c.4451C>G	XP_011541375.1:p.Thr1484Ser
XM_011543074.1:c.4064C>G	XP_011541376.1:p.Thr1355Ser
XM_011543075.1:c.3728C>G	XP_011541377.1:p.Thr1243Ser
XM_005271736.4:c.4745C>G	XP_005271793.2:p.Thr1582Ser
XM_011543072.2:c.4625C>G	XP_011541374.1:p.Thr1542Ser
XM_011543073.2:c.4664C>G	XP_011541375.2:p.Thr1555Ser
XM_011543075.2:c.3728C>G	XP_011541377.1:p.Thr1243Ser
XM_017018595.2:c.4625C>G	XP_016874084.1:p.Thr1542Ser
XM_017018596.1:c.4466C>G	XP_016874085.1:p.Thr1489Ser
NM_014715.4:c.3656C>G	NP_055530.2:p.Thr1219Ser
NM_001142685.2:c.4703C>G	NP_001136157.1:p.Thr1568Ser
NM_001378024.1:c.4745C>G MANE Select	NP_001364953.1:p.Thr1582Ser
NM_001378025.1:c.4583C>G	NP_001364954.1:p.Thr1528Ser