Canonical Allele Identifier: CA187670153

Gene: ARHGAP39

Linked Data

• dbSNP Id: rs539911717
• gnomAD v2: 8-145778059-A-AT
• gnomAD v3: 8-144552675-A-AT
• gnomAD v4: 8-144552675-A-AT
• MyVariant Identifiers: chr8:g.145778060_145778061insT (hg19) ; chr8:g.145778059_145778060insT (hg19) ; chr8:g.144552676_144552677insT (hg38) ; chr8:g.144552675_144552676insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144552684dup , CM000670.2:g.144552684dup	GRCh38
NC_000008.10:g.145778068dup , CM000670.1:g.145778068dup	GRCh37
NC_000008.9:g.145748876dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000377307.7:c.596+2884dup MANE Select	ENSP00000366522.2:n.596+2884dup
ENST00000276826.5:c.596+2884dup	ENSP00000276826.5:n.596+2884dup
ENST00000377307.6:c.596+2884dup	ENSP00000366522.2:n.596+2884dup
NM_001308207.1:c.596+2884dup	NP_001295136.1:n.596+2884dup
NM_001308208.1:c.596+2884dup	NP_001295137.1:n.596+2884dup
NM_025251.1:c.596+2884dup	NP_079527.1:n.596+2884dup
NM_025251.2:c.596+2884dup	NP_079527.1:n.596+2884dup
XM_011517308.1:c.596+2884dup	XP_011515610.1:n.596+2884dup
XM_011517309.1:c.596+2884dup	XP_011515611.1:n.596+2884dup
XM_011517311.1:c.164+2884dup	XP_011515613.1:n.164+2884dup
XM_011517312.1:c.125+2884dup	XP_011515614.1:n.125+2884dup
XM_011517309.2:c.596+2884dup	XP_011515611.1:n.596+2884dup
XM_011517312.2:c.125+2884dup	XP_011515614.1:n.125+2884dup
XM_017013870.2:c.596+2884dup	XP_016869359.1:n.596+2884dup
NM_001308208.2:c.596+2884dup	NP_001295137.1:n.596+2884dup
NM_025251.3:c.596+2884dup MANE Select	NP_079527.1:n.596+2884dup