Canonical Allele Identifier: CA1144795927
Gene: ARHGAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94209096G= , CM000663.2:g.94209096G= GRCh38
NC_000001.10:g.94674652G= , CM000663.1:g.94674652G= GRCh37
NC_000001.9:g.94447240G= NCBI36
NG_050965.1:g.70973C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260526.11:c.437+158C= MANE Select ENSP00000260526.6:n.437+158C=
ENST00000260526.10:c.437+158C= ENSP00000260526.6:n.437+158C=
ENST00000370217.3:c.437+158C= ENSP00000359237.3:n.437+158C=
ENST00000552844.5:c.437+158C= ENSP00000449764.1:n.437+158C=
NM_004815.3:c.437+158C= NP_004806.3:n.437+158C=
XM_006711048.2:c.245+158C= XP_006711111.1:n.245+158C=
XM_011542438.1:c.437+158C= XP_011540740.1:n.437+158C=
XM_011542439.1:c.437+158C= XP_011540741.1:n.437+158C=
XM_011542440.1:c.245+158C= XP_011540742.1:n.245+158C=
NM_001328664.1:c.437+158C= NP_001315593.1:n.437+158C=
NM_001328665.1:c.245+158C= NP_001315594.1:n.245+158C=
NM_001328666.1:c.437+158C= NP_001315595.1:n.437+158C=
NM_001328667.1:c.245+158C= NP_001315596.1:n.245+158C=
XM_011542439.2:c.437+158C= XP_011540741.1:n.437+158C=
NM_004815.4:c.437+158C= MANE Select NP_004806.3:n.437+158C=
NM_001328664.2:c.437+158C= NP_001315593.1:n.437+158C=
NM_001328665.2:c.245+158C= NP_001315594.1:n.245+158C=
NM_001328666.2:c.437+158C= NP_001315595.1:n.437+158C=
NM_001328667.2:c.245+158C= NP_001315596.1:n.245+158C=