Canonical Allele Identifier: CA2284923504

Gene: GNAL

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11752494C= , CM000680.2:g.11752494C=	GRCh38
NC_000018.9:g.11752493C= , CM000680.1:g.11752493C=	GRCh37
NC_000018.8:g.11742493C=	NCBI36
NG_033866.1:g.68480C=

Transcript Alleles

HGVS	Amino-acid Change
NM_182978.4:c.377-359C= MANE Select	NP_892023.1:n.377-359C=
ENST00000334049.11:c.377-359C= MANE Select	ENSP00000334051.5:n.377-359C=
NM_001369387.1:c.61C= MANE Plus Clinical	NP_001356316.1:p.Arg21=
ENST00000423027.8:c.61C= MANE Plus Clinical	ENSP00000408489.2:p.Arg21=
NM_001142339.2:c.61C=	NP_001135811.1:p.Arg21=
NM_001142339.3:c.61C=	NP_001135811.1:p.Arg21=
NM_001261443.1:c.61C=	NP_001248372.1:p.Arg21=
NM_001261443.2:c.61C=	NP_001248372.1:p.Arg21=
NM_182978.3:c.377-359C=	NP_892023.1:n.377-359C=
ENST00000269162.9:c.61C=	ENSP00000269162.4:p.Arg21=
ENST00000334049.10:c.377-359C=	ENSP00000334051.5:n.377-359C=
ENST00000423027.7:c.61C=	ENSP00000408489.2:p.Arg21=
ENST00000535121.5:c.61C=	ENSP00000439023.1:p.Arg21=
XM_006722323.2:c.61C=	XP_006722386.1:p.Arg21=
XM_006722324.1:c.377-359C=	XP_006722387.1:n.377-359C=
XM_006722324.3:c.377-359C=	XP_006722387.1:n.377-359C=
XM_011525654.1:c.61C=	XP_011523956.1:p.Arg21=
XM_024451164.1:c.61C=	XP_024306932.1:p.Arg21=