Canonical Allele Identifier: CA2744624101

Gene: ARHGAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94209081_94209082insTCGA , CM000663.2:g.94209081_94209082insTCGA	GRCh38
NC_000001.10:g.94674637_94674638insTCGA , CM000663.1:g.94674637_94674638insTCGA	GRCh37
NC_000001.9:g.94447225_94447226insTCGA	NCBI36
NG_050965.1:g.70987_70988insTCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260526.11:c.437+172_437+173insTCGA MANE Select	ENSP00000260526.6:n.437+172_437+173insTCGA
ENST00000260526.10:c.437+172_437+173insTCGA	ENSP00000260526.6:n.437+172_437+173insTCGA
ENST00000370217.3:c.437+172_437+173insTCGA	ENSP00000359237.3:n.437+172_437+173insTCGA
ENST00000552844.5:c.437+172_437+173insTCGA	ENSP00000449764.1:n.437+172_437+173insTCGA
NM_004815.3:c.437+172_437+173insTCGA	NP_004806.3:n.437+172_437+173insTCGA
XM_006711048.2:c.245+172_245+173insTCGA	XP_006711111.1:n.245+172_245+173insTCGA
XM_011542438.1:c.437+172_437+173insTCGA	XP_011540740.1:n.437+172_437+173insTCGA
XM_011542439.1:c.437+172_437+173insTCGA	XP_011540741.1:n.437+172_437+173insTCGA
XM_011542440.1:c.245+172_245+173insTCGA	XP_011540742.1:n.245+172_245+173insTCGA
NM_001328664.1:c.437+172_437+173insTCGA	NP_001315593.1:n.437+172_437+173insTCGA
NM_001328665.1:c.245+172_245+173insTCGA	NP_001315594.1:n.245+172_245+173insTCGA
NM_001328666.1:c.437+172_437+173insTCGA	NP_001315595.1:n.437+172_437+173insTCGA
NM_001328667.1:c.245+172_245+173insTCGA	NP_001315596.1:n.245+172_245+173insTCGA
XM_011542439.2:c.437+172_437+173insTCGA	XP_011540741.1:n.437+172_437+173insTCGA
NM_004815.4:c.437+172_437+173insTCGA MANE Select	NP_004806.3:n.437+172_437+173insTCGA
NM_001328664.2:c.437+172_437+173insTCGA	NP_001315593.1:n.437+172_437+173insTCGA
NM_001328665.2:c.245+172_245+173insTCGA	NP_001315594.1:n.245+172_245+173insTCGA
NM_001328666.2:c.437+172_437+173insTCGA	NP_001315595.1:n.437+172_437+173insTCGA
NM_001328667.2:c.245+172_245+173insTCGA	NP_001315596.1:n.245+172_245+173insTCGA