Canonical Allele Identifier: CA2284983226
Gene: GNAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.11880951G= , CM000680.2:g.11880951G= GRCh38
NC_000018.9:g.11880950G= , CM000680.1:g.11880950G= GRCh37
NC_000018.8:g.11870950G= NCBI36
NG_033866.1:g.196937G=

Transcript Alleles

HGVS Amino-acid change
ENST00000334049.11:c.1231-38G= MANE Select ENSP00000334051.5:n.1231-38G=
ENST00000423027.8:c.1000-38G= MANE Plus Clinical ENSP00000408489.2:n.1000-38G=
ENST00000269162.9:c.1000-38G= ENSP00000269162.4:n.1000-38G=
ENST00000334049.10:c.1231-38G= ENSP00000334051.5:n.1231-38G=
ENST00000423027.7:c.1000-38G= ENSP00000408489.2:n.1000-38G=
ENST00000535121.5:c.1000-38G= ENSP00000439023.1:n.1000-38G=
ENST00000602628.1:c.379-38G= ENSP00000473600.1:n.379-38G=
NM_001142339.2:c.1000-38G= NP_001135811.1:n.1000-38G=
NM_001261443.1:c.1000-38G= NP_001248372.1:n.1000-38G=
NM_001261444.1:c.379-38G= NP_001248373.1:n.379-38G=
NM_182978.3:c.1231-38G= NP_892023.1:n.1231-38G=
XM_006722323.2:c.1000-38G= XP_006722386.1:n.1000-38G=
XM_011525654.1:c.1000-38G= XP_011523956.1:n.1000-38G=
XM_024451164.1:c.1000-38G= XP_024306932.1:n.1000-38G=
NM_182978.4:c.1231-38G= MANE Select NP_892023.1:n.1231-38G=
NM_001261444.2:c.379-38G= NP_001248373.1:n.379-38G=
NM_001369387.1:c.1000-38G= MANE Plus Clinical NP_001356316.1:n.1000-38G=
NM_001142339.3:c.1000-38G= NP_001135811.1:n.1000-38G=
NM_001261443.2:c.1000-38G= NP_001248372.1:n.1000-38G=