Canonical Allele Identifier: CA1181488434
Gene: ARHGAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94209077T= , CM000663.2:g.94209077T= GRCh38
NC_000001.10:g.94674633T= , CM000663.1:g.94674633T= GRCh37
NC_000001.9:g.94447221T= NCBI36
NG_050965.1:g.70992A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260526.11:c.438-173A= MANE Select ENSP00000260526.6:n.438-173A=
ENST00000260526.10:c.438-173A= ENSP00000260526.6:n.438-173A=
ENST00000370217.3:c.438-173A= ENSP00000359237.3:n.438-173A=
ENST00000552844.5:c.438-173A= ENSP00000449764.1:n.438-173A=
NM_004815.3:c.438-173A= NP_004806.3:n.438-173A=
XM_006711048.2:c.246-173A= XP_006711111.1:n.246-173A=
XM_011542438.1:c.438-173A= XP_011540740.1:n.438-173A=
XM_011542439.1:c.438-173A= XP_011540741.1:n.438-173A=
XM_011542440.1:c.246-173A= XP_011540742.1:n.246-173A=
NM_001328664.1:c.438-173A= NP_001315593.1:n.438-173A=
NM_001328665.1:c.246-173A= NP_001315594.1:n.246-173A=
NM_001328666.1:c.438-173A= NP_001315595.1:n.438-173A=
NM_001328667.1:c.246-173A= NP_001315596.1:n.246-173A=
XM_011542439.2:c.438-173A= XP_011540741.1:n.438-173A=
NM_004815.4:c.438-173A= MANE Select NP_004806.3:n.438-173A=
NM_001328664.2:c.438-173A= NP_001315593.1:n.438-173A=
NM_001328665.2:c.246-173A= NP_001315594.1:n.246-173A=
NM_001328666.2:c.438-173A= NP_001315595.1:n.438-173A=
NM_001328667.2:c.246-173A= NP_001315596.1:n.246-173A=