Canonical Allele Identifier: CA2284983865

Gene: GNAL

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11882190T= , CM000680.2:g.11882190T=	GRCh38
NC_000018.9:g.11882189T= , CM000680.1:g.11882189T=	GRCh37
NC_000018.8:g.11872189T=	NCBI36
NG_033866.1:g.198176T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.*1055T= MANE Select	ENSP00000334051.5:n.*1055T=
ENST00000423027.8:c.*1055T= MANE Plus Clinical	ENSP00000408489.2:n.*1055T=
ENST00000334049.10:c.*1055T=	ENSP00000334051.5:n.*1055T=
NM_001142339.2:c.*1055T=	NP_001135811.1:n.*1055T=
NM_001261443.1:c.*1055T=	NP_001248372.1:n.*1055T=
NM_001261444.1:c.*1055T=	NP_001248373.1:n.*1055T=
NM_182978.3:c.*1055T=	NP_892023.1:n.*1055T=
XM_024451164.1:c.*1055T=	XP_024306932.1:n.*1055T=
NM_182978.4:c.*1055T= MANE Select	NP_892023.1:n.*1055T=
NM_001261444.2:c.*1055T=	NP_001248373.1:n.*1055T=
NM_001369387.1:c.*1055T= MANE Plus Clinical	NP_001356316.1:n.*1055T=
NM_001142339.3:c.*1055T=	NP_001135811.1:n.*1055T=
NM_001261443.2:c.*1055T=	NP_001248372.1:n.*1055T=