Canonical Allele Identifier: CA14510239

Gene: GNAL

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11751989T>G , CM000680.2:g.11751989T>G	GRCh38
NC_000018.9:g.11751988T>G , CM000680.1:g.11751988T>G	GRCh37
NC_000018.8:g.11741988T>G	NCBI36
NG_033866.1:g.67975T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_182978.4:c.377-864T>G MANE Select	NP_892023.1:n.377-864T>G
ENST00000334049.11:c.377-864T>G MANE Select	ENSP00000334051.5:n.377-864T>G
NM_001142339.2:c.-103+283T>G	NP_001135811.1:n.-103+283T>G
NM_001142339.3:c.-103+283T>G	NP_001135811.1:n.-103+283T>G
NM_001261443.1:c.-102-343T>G	NP_001248372.1:n.-102-343T>G
NM_001261443.2:c.-102-343T>G	NP_001248372.1:n.-102-343T>G
NM_182978.3:c.377-864T>G	NP_892023.1:n.377-864T>G
ENST00000269162.9:c.-103+283T>G	ENSP00000269162.4:n.-103+283T>G
ENST00000334049.10:c.377-864T>G	ENSP00000334051.5:n.377-864T>G
ENST00000535121.5:c.-102-343T>G	ENSP00000439023.1:n.-102-343T>G
XM_006722324.1:c.377-864T>G	XP_006722387.1:n.377-864T>G
XM_006722324.3:c.377-864T>G	XP_006722387.1:n.377-864T>G
XM_011525654.1:c.-106+283T>G	XP_011523956.1:n.-106+283T>G
XM_024451164.1:c.-445T>G	XP_024306932.1:n.-445T>G