Canonical Allele Identifier: CA2641033582

Gene: GNAL

Linked Data

• gnomAD v4: 18-11880889-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11880890dup , CM000680.2:g.11880890dup	GRCh38
NC_000018.9:g.11880889dup , CM000680.1:g.11880889dup	GRCh37
NC_000018.8:g.11870889dup	NCBI36
NG_033866.1:g.196876dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.1231-99dup MANE Select	ENSP00000334051.5:n.1231-99dup
ENST00000423027.8:c.1000-99dup MANE Plus Clinical	ENSP00000408489.2:n.1000-99dup
ENST00000269162.9:c.1000-99dup	ENSP00000269162.4:n.1000-99dup
ENST00000334049.10:c.1231-99dup	ENSP00000334051.5:n.1231-99dup
ENST00000423027.7:c.1000-99dup	ENSP00000408489.2:n.1000-99dup
ENST00000535121.5:c.1000-99dup	ENSP00000439023.1:n.1000-99dup
ENST00000602628.1:c.379-99dup	ENSP00000473600.1:n.379-99dup
NM_001142339.2:c.1000-99dup	NP_001135811.1:n.1000-99dup
NM_001261443.1:c.1000-99dup	NP_001248372.1:n.1000-99dup
NM_001261444.1:c.379-99dup	NP_001248373.1:n.379-99dup
NM_182978.3:c.1231-99dup	NP_892023.1:n.1231-99dup
XM_006722323.2:c.1000-99dup	XP_006722386.1:n.1000-99dup
XM_011525654.1:c.1000-99dup	XP_011523956.1:n.1000-99dup
XM_024451164.1:c.1000-99dup	XP_024306932.1:n.1000-99dup
NM_182978.4:c.1231-99dup MANE Select	NP_892023.1:n.1231-99dup
NM_001261444.2:c.379-99dup	NP_001248373.1:n.379-99dup
NM_001369387.1:c.1000-99dup MANE Plus Clinical	NP_001356316.1:n.1000-99dup
NM_001142339.3:c.1000-99dup	NP_001135811.1:n.1000-99dup
NM_001261443.2:c.1000-99dup	NP_001248372.1:n.1000-99dup