Canonical Allele Identifier: CA2284983275
Gene: GNAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.11881063C= , CM000680.2:g.11881063C= GRCh38
NC_000018.9:g.11881062C= , CM000680.1:g.11881062C= GRCh37
NC_000018.8:g.11871062C= NCBI36
NG_033866.1:g.197049C=

Transcript Alleles

HGVS Amino-acid change
ENST00000334049.11:c.1305C= MANE Select ENSP00000334051.5:p.Asn435=
ENST00000423027.8:c.1074C= MANE Plus Clinical ENSP00000408489.2:p.Asn358=
ENST00000269162.9:c.1074C= ENSP00000269162.4:p.Asn358=
ENST00000334049.10:c.1305C= ENSP00000334051.5:p.Asn435=
ENST00000423027.7:c.1074C= ENSP00000408489.2:p.Asn358=
ENST00000535121.5:c.1074C= ENSP00000439023.1:p.Asn358=
ENST00000602628.1:c.453C= ENSP00000473600.1:p.Asn151=
NM_001142339.2:c.1074C= NP_001135811.1:p.Asn358=
NM_001261443.1:c.1074C= NP_001248372.1:p.Asn358=
NM_001261444.1:c.453C= NP_001248373.1:p.Asn151=
NM_182978.3:c.1305C= NP_892023.1:p.Asn435=
XM_006722323.2:c.1074C= XP_006722386.1:p.Asn358=
XM_011525654.1:c.1074C= XP_011523956.1:p.Asn358=
XM_024451164.1:c.1074C= XP_024306932.1:p.Asn358=
NM_182978.4:c.1305C= MANE Select NP_892023.1:p.Asn435=
NM_001261444.2:c.453C= NP_001248373.1:p.Asn151=
NM_001369387.1:c.1074C= MANE Plus Clinical NP_001356316.1:p.Asn358=
NM_001142339.3:c.1074C= NP_001135811.1:p.Asn358=
NM_001261443.2:c.1074C= NP_001248372.1:p.Asn358=