Canonical Allele Identifier: CA2641034282

Gene: GNAL

Linked Data

• gnomAD v4: 18-11882029-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11882029G>T , CM000680.2:g.11882029G>T	GRCh38
NC_000018.9:g.11882028G>T , CM000680.1:g.11882028G>T	GRCh37
NC_000018.8:g.11872028G>T	NCBI36
NG_033866.1:g.198015G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.*894G>T MANE Select	ENSP00000334051.5:n.*894G>T
ENST00000423027.8:c.*894G>T MANE Plus Clinical	ENSP00000408489.2:n.*894G>T
ENST00000334049.10:c.*894G>T	ENSP00000334051.5:n.*894G>T
NM_001142339.2:c.*894G>T	NP_001135811.1:n.*894G>T
NM_001261443.1:c.*894G>T	NP_001248372.1:n.*894G>T
NM_001261444.1:c.*894G>T	NP_001248373.1:n.*894G>T
NM_182978.3:c.*894G>T	NP_892023.1:n.*894G>T
XM_024451164.1:c.*894G>T	XP_024306932.1:n.*894G>T
NM_182978.4:c.*894G>T MANE Select	NP_892023.1:n.*894G>T
NM_001261444.2:c.*894G>T	NP_001248373.1:n.*894G>T
NM_001369387.1:c.*894G>T MANE Plus Clinical	NP_001356316.1:n.*894G>T
NM_001142339.3:c.*894G>T	NP_001135811.1:n.*894G>T
NM_001261443.2:c.*894G>T	NP_001248372.1:n.*894G>T