Canonical Allele Identifier: CA2284983800

Gene: GNAL

Linked Data

• dbSNP Id: rs2036706980

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11882069_11882071dup , CM000680.2:g.11882069_11882071dup	GRCh38
NC_000018.9:g.11882068_11882070dup , CM000680.1:g.11882068_11882070dup	GRCh37
NC_000018.8:g.11872068_11872070dup	NCBI36
NG_033866.1:g.198055_198057dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334049.11:c.*934_*936dup MANE Select	ENSP00000334051.5:n.*934_*936dup
ENST00000423027.8:c.*934_*936dup MANE Plus Clinical	ENSP00000408489.2:n.*934_*936dup
ENST00000334049.10:c.*934_*936dup	ENSP00000334051.5:n.*934_*936dup
NM_001142339.2:c.*934_*936dup	NP_001135811.1:n.*934_*936dup
NM_001261443.1:c.*934_*936dup	NP_001248372.1:n.*934_*936dup
NM_001261444.1:c.*934_*936dup	NP_001248373.1:n.*934_*936dup
NM_182978.3:c.*934_*936dup	NP_892023.1:n.*934_*936dup
XM_024451164.1:c.*934_*936dup	XP_024306932.1:n.*934_*936dup
NM_182978.4:c.*934_*936dup MANE Select	NP_892023.1:n.*934_*936dup
NM_001261444.2:c.*934_*936dup	NP_001248373.1:n.*934_*936dup
NM_001369387.1:c.*934_*936dup MANE Plus Clinical	NP_001356316.1:n.*934_*936dup
NM_001142339.3:c.*934_*936dup	NP_001135811.1:n.*934_*936dup
NM_001261443.2:c.*934_*936dup	NP_001248372.1:n.*934_*936dup