Canonical Allele Identifier: CA776157627

Gene: GNAL

Linked Data

• dbSNP Id: rs1220507976
• MyVariant Identifiers: chr18:g.11882184A>C (hg19) ; chr18:g.11882185A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11882185A>C , CM000680.2:g.11882185A>C	GRCh38
NC_000018.9:g.11882184A>C , CM000680.1:g.11882184A>C	GRCh37
NC_000018.8:g.11872184A>C	NCBI36
NG_033866.1:g.198171A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.*1050A>C MANE Select	ENSP00000334051.5:n.*1050A>C
ENST00000423027.8:c.*1050A>C MANE Plus Clinical	ENSP00000408489.2:n.*1050A>C
ENST00000334049.10:c.*1050A>C	ENSP00000334051.5:n.*1050A>C
NM_001142339.2:c.*1050A>C	NP_001135811.1:n.*1050A>C
NM_001261443.1:c.*1050A>C	NP_001248372.1:n.*1050A>C
NM_001261444.1:c.*1050A>C	NP_001248373.1:n.*1050A>C
NM_182978.3:c.*1050A>C	NP_892023.1:n.*1050A>C
XM_024451164.1:c.*1050A>C	XP_024306932.1:n.*1050A>C
NM_182978.4:c.*1050A>C MANE Select	NP_892023.1:n.*1050A>C
NM_001261444.2:c.*1050A>C	NP_001248373.1:n.*1050A>C
NM_001369387.1:c.*1050A>C MANE Plus Clinical	NP_001356316.1:n.*1050A>C
NM_001142339.3:c.*1050A>C	NP_001135811.1:n.*1050A>C
NM_001261443.2:c.*1050A>C	NP_001248372.1:n.*1050A>C