Canonical Allele Identifier: CA502927800

Gene: GNAL

Linked Data

• MyVariant Identifiers: chr18:g.11881050G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11881051G>T , CM000680.2:g.11881051G>T	GRCh38
NC_000018.9:g.11881050G>T , CM000680.1:g.11881050G>T	GRCh37
NC_000018.8:g.11871050G>T	NCBI36
NG_033866.1:g.197037G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334049.11:c.1293G>T MANE Select	ENSP00000334051.5:p.Val431=
ENST00000423027.8:c.1062G>T MANE Plus Clinical	ENSP00000408489.2:p.Val354=
ENST00000269162.9:c.1062G>T	ENSP00000269162.4:p.Val354=
ENST00000334049.10:c.1293G>T	ENSP00000334051.5:p.Val431=
ENST00000423027.7:c.1062G>T	ENSP00000408489.2:p.Val354=
ENST00000535121.5:c.1062G>T	ENSP00000439023.1:p.Val354=
ENST00000602628.1:c.441G>T	ENSP00000473600.1:p.Val147=
NM_001142339.2:c.1062G>T	NP_001135811.1:p.Val354=
NM_001261443.1:c.1062G>T	NP_001248372.1:p.Val354=
NM_001261444.1:c.441G>T	NP_001248373.1:p.Val147=
NM_182978.3:c.1293G>T	NP_892023.1:p.Val431=
XM_006722323.2:c.1062G>T	XP_006722386.1:p.Val354=
XM_011525654.1:c.1062G>T	XP_011523956.1:p.Val354=
XM_024451164.1:c.1062G>T	XP_024306932.1:p.Val354=
NM_182978.4:c.1293G>T MANE Select	NP_892023.1:p.Val431=
NM_001261444.2:c.441G>T	NP_001248373.1:p.Val147=
NM_001369387.1:c.1062G>T MANE Plus Clinical	NP_001356316.1:p.Val354=
NM_001142339.3:c.1062G>T	NP_001135811.1:p.Val354=
NM_001261443.2:c.1062G>T	NP_001248372.1:p.Val354=