Canonical Allele Identifier: CA2810989422

Gene: GNAL

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11881940C>A , CM000680.2:g.11881940C>A	GRCh38
NC_000018.9:g.11881939C>A , CM000680.1:g.11881939C>A	GRCh37
NC_000018.8:g.11871939C>A	NCBI36
NG_033866.1:g.197926C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.*805C>A MANE Select	ENSP00000334051.5:n.*805C>A
ENST00000423027.8:c.*805C>A MANE Plus Clinical	ENSP00000408489.2:n.*805C>A
ENST00000334049.10:c.*805C>A	ENSP00000334051.5:n.*805C>A
NM_001142339.2:c.*805C>A	NP_001135811.1:n.*805C>A
NM_001261443.1:c.*805C>A	NP_001248372.1:n.*805C>A
NM_001261444.1:c.*805C>A	NP_001248373.1:n.*805C>A
NM_182978.3:c.*805C>A	NP_892023.1:n.*805C>A
XM_024451164.1:c.*805C>A	XP_024306932.1:n.*805C>A
NM_182978.4:c.*805C>A MANE Select	NP_892023.1:n.*805C>A
NM_001261444.2:c.*805C>A	NP_001248373.1:n.*805C>A
NM_001369387.1:c.*805C>A MANE Plus Clinical	NP_001356316.1:n.*805C>A
NM_001142339.3:c.*805C>A	NP_001135811.1:n.*805C>A
NM_001261443.2:c.*805C>A	NP_001248372.1:n.*805C>A