Canonical Allele Identifier: CA1826389788

Gene: ARHGAP39

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144552675A= , CM000670.2:g.144552675A=	GRCh38
NC_000008.10:g.145778059A= , CM000670.1:g.145778059A=	GRCh37
NC_000008.9:g.145748867A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000377307.7:c.596+2885T= MANE Select	ENSP00000366522.2:n.596+2885T=
ENST00000276826.5:c.596+2885T=	ENSP00000276826.5:n.596+2885T=
ENST00000377307.6:c.596+2885T=	ENSP00000366522.2:n.596+2885T=
NM_001308207.1:c.596+2885T=	NP_001295136.1:n.596+2885T=
NM_001308208.1:c.596+2885T=	NP_001295137.1:n.596+2885T=
NM_025251.1:c.596+2885T=	NP_079527.1:n.596+2885T=
NM_025251.2:c.596+2885T=	NP_079527.1:n.596+2885T=
XM_011517308.1:c.596+2885T=	XP_011515610.1:n.596+2885T=
XM_011517309.1:c.596+2885T=	XP_011515611.1:n.596+2885T=
XM_011517311.1:c.164+2885T=	XP_011515613.1:n.164+2885T=
XM_011517312.1:c.125+2885T=	XP_011515614.1:n.125+2885T=
XM_011517309.2:c.596+2885T=	XP_011515611.1:n.596+2885T=
XM_011517312.2:c.125+2885T=	XP_011515614.1:n.125+2885T=
XM_017013870.2:c.596+2885T=	XP_016869359.1:n.596+2885T=
NM_001308208.2:c.596+2885T=	NP_001295137.1:n.596+2885T=
NM_025251.3:c.596+2885T= MANE Select	NP_079527.1:n.596+2885T=