Canonical Allele Identifier: CA776157526

Gene: GNAL

Linked Data

• dbSNP Id: rs1163324046
• gnomAD v3: 18-11882040-G-T
• gnomAD v4: 18-11882040-G-T
• MyVariant Identifiers: chr18:g.11882039G>T (hg19) ; chr18:g.11882040G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11882040G>T , CM000680.2:g.11882040G>T	GRCh38
NC_000018.9:g.11882039G>T , CM000680.1:g.11882039G>T	GRCh37
NC_000018.8:g.11872039G>T	NCBI36
NG_033866.1:g.198026G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.*905G>T MANE Select	ENSP00000334051.5:n.*905G>T
ENST00000423027.8:c.*905G>T MANE Plus Clinical	ENSP00000408489.2:n.*905G>T
ENST00000334049.10:c.*905G>T	ENSP00000334051.5:n.*905G>T
NM_001142339.2:c.*905G>T	NP_001135811.1:n.*905G>T
NM_001261443.1:c.*905G>T	NP_001248372.1:n.*905G>T
NM_001261444.1:c.*905G>T	NP_001248373.1:n.*905G>T
NM_182978.3:c.*905G>T	NP_892023.1:n.*905G>T
XM_024451164.1:c.*905G>T	XP_024306932.1:n.*905G>T
NM_182978.4:c.*905G>T MANE Select	NP_892023.1:n.*905G>T
NM_001261444.2:c.*905G>T	NP_001248373.1:n.*905G>T
NM_001369387.1:c.*905G>T MANE Plus Clinical	NP_001356316.1:n.*905G>T
NM_001142339.3:c.*905G>T	NP_001135811.1:n.*905G>T
NM_001261443.2:c.*905G>T	NP_001248372.1:n.*905G>T