Canonical Allele Identifier: CA2641033652

Gene: GNAL

Linked Data

• gnomAD v4: 18-11881146-GCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11881149_11881151del , CM000680.2:g.11881149_11881151del	GRCh38
NC_000018.9:g.11881148_11881150del , CM000680.1:g.11881148_11881150del	GRCh37
NC_000018.8:g.11871148_11871150del	NCBI36
NG_033866.1:g.197135_197137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.*14_*16del MANE Select	ENSP00000334051.5:n.*14_*16del
ENST00000423027.8:c.*14_*16del MANE Plus Clinical	ENSP00000408489.2:n.*14_*16del
ENST00000269162.9:c.*14_*16del	ENSP00000269162.4:n.*14_*16del
ENST00000334049.10:c.*14_*16del	ENSP00000334051.5:n.*14_*16del
ENST00000423027.7:c.*14_*16del	ENSP00000408489.2:n.*14_*16del
ENST00000602628.1:c.*14_*16del	ENSP00000473600.1:n.*14_*16del
NM_001142339.2:c.*14_*16del	NP_001135811.1:n.*14_*16del
NM_001261443.1:c.*14_*16del	NP_001248372.1:n.*14_*16del
NM_001261444.1:c.*14_*16del	NP_001248373.1:n.*14_*16del
NM_182978.3:c.*14_*16del	NP_892023.1:n.*14_*16del
XM_006722323.2:c.*14_*16del	XP_006722386.1:n.*14_*16del
XM_011525654.1:c.*14_*16del	XP_011523956.1:n.*14_*16del
XM_024451164.1:c.*14_*16del	XP_024306932.1:n.*14_*16del
NM_182978.4:c.*14_*16del MANE Select	NP_892023.1:n.*14_*16del
NM_001261444.2:c.*14_*16del	NP_001248373.1:n.*14_*16del
NM_001369387.1:c.*14_*16del MANE Plus Clinical	NP_001356316.1:n.*14_*16del
NM_001142339.3:c.*14_*16del	NP_001135811.1:n.*14_*16del
NM_001261443.2:c.*14_*16del	NP_001248372.1:n.*14_*16del