Canonical Allele Identifier: CA1181488446

Gene: ARHGAP29

Linked Data

• dbSNP Id: rs1651409517

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94209106del , CM000663.2:g.94209106del	GRCh38
NC_000001.10:g.94674662del , CM000663.1:g.94674662del	GRCh37
NC_000001.9:g.94447250del	NCBI36
NG_050965.1:g.70964del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260526.11:c.437+149del MANE Select	ENSP00000260526.6:n.437+149del
ENST00000260526.10:c.437+149del	ENSP00000260526.6:n.437+149del
ENST00000370217.3:c.437+149del	ENSP00000359237.3:n.437+149del
ENST00000552844.5:c.437+149del	ENSP00000449764.1:n.437+149del
NM_004815.3:c.437+149del	NP_004806.3:n.437+149del
XM_006711048.2:c.245+149del	XP_006711111.1:n.245+149del
XM_011542438.1:c.437+149del	XP_011540740.1:n.437+149del
XM_011542439.1:c.437+149del	XP_011540741.1:n.437+149del
XM_011542440.1:c.245+149del	XP_011540742.1:n.245+149del
NM_001328664.1:c.437+149del	NP_001315593.1:n.437+149del
NM_001328665.1:c.245+149del	NP_001315594.1:n.245+149del
NM_001328666.1:c.437+149del	NP_001315595.1:n.437+149del
NM_001328667.1:c.245+149del	NP_001315596.1:n.245+149del
XM_011542439.2:c.437+149del	XP_011540741.1:n.437+149del
NM_004815.4:c.437+149del MANE Select	NP_004806.3:n.437+149del
NM_001328664.2:c.437+149del	NP_001315593.1:n.437+149del
NM_001328665.2:c.245+149del	NP_001315594.1:n.245+149del
NM_001328666.2:c.437+149del	NP_001315595.1:n.437+149del
NM_001328667.2:c.245+149del	NP_001315596.1:n.245+149del