Canonical Allele Identifier: CA2284983773

Gene: GNAL

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11881996T= , CM000680.2:g.11881996T=	GRCh38
NC_000018.9:g.11881995T= , CM000680.1:g.11881995T=	GRCh37
NC_000018.8:g.11871995T=	NCBI36
NG_033866.1:g.197982T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.*861T= MANE Select	ENSP00000334051.5:n.*861T=
ENST00000423027.8:c.*861T= MANE Plus Clinical	ENSP00000408489.2:n.*861T=
ENST00000334049.10:c.*861T=	ENSP00000334051.5:n.*861T=
NM_001142339.2:c.*861T=	NP_001135811.1:n.*861T=
NM_001261443.1:c.*861T=	NP_001248372.1:n.*861T=
NM_001261444.1:c.*861T=	NP_001248373.1:n.*861T=
NM_182978.3:c.*861T=	NP_892023.1:n.*861T=
XM_024451164.1:c.*861T=	XP_024306932.1:n.*861T=
NM_182978.4:c.*861T= MANE Select	NP_892023.1:n.*861T=
NM_001261444.2:c.*861T=	NP_001248373.1:n.*861T=
NM_001369387.1:c.*861T= MANE Plus Clinical	NP_001356316.1:n.*861T=
NM_001142339.3:c.*861T=	NP_001135811.1:n.*861T=
NM_001261443.2:c.*861T=	NP_001248372.1:n.*861T=