Canonical Allele Identifier: CA1142481811

Gene: ARHGAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94209072C= , CM000663.2:g.94209072C=	GRCh38
NC_000001.10:g.94674628C= , CM000663.1:g.94674628C=	GRCh37
NC_000001.9:g.94447216C=	NCBI36
NG_050965.1:g.70997G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260526.11:c.438-168G= MANE Select	ENSP00000260526.6:n.438-168G=
ENST00000260526.10:c.438-168G=	ENSP00000260526.6:n.438-168G=
ENST00000370217.3:c.438-168G=	ENSP00000359237.3:n.438-168G=
ENST00000552844.5:c.438-168G=	ENSP00000449764.1:n.438-168G=
NM_004815.3:c.438-168G=	NP_004806.3:n.438-168G=
XM_006711048.2:c.246-168G=	XP_006711111.1:n.246-168G=
XM_011542438.1:c.438-168G=	XP_011540740.1:n.438-168G=
XM_011542439.1:c.438-168G=	XP_011540741.1:n.438-168G=
XM_011542440.1:c.246-168G=	XP_011540742.1:n.246-168G=
NM_001328664.1:c.438-168G=	NP_001315593.1:n.438-168G=
NM_001328665.1:c.246-168G=	NP_001315594.1:n.246-168G=
NM_001328666.1:c.438-168G=	NP_001315595.1:n.438-168G=
NM_001328667.1:c.246-168G=	NP_001315596.1:n.246-168G=
XM_011542439.2:c.438-168G=	XP_011540741.1:n.438-168G=
NM_004815.4:c.438-168G= MANE Select	NP_004806.3:n.438-168G=
NM_001328664.2:c.438-168G=	NP_001315593.1:n.438-168G=
NM_001328665.2:c.246-168G=	NP_001315594.1:n.246-168G=
NM_001328666.2:c.438-168G=	NP_001315595.1:n.438-168G=
NM_001328667.2:c.246-168G=	NP_001315596.1:n.246-168G=