Canonical Allele Identifier: CA347266969

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717109A>G (hg19) ; chr2:g.73489982A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489982A>G , CM000664.2:g.73489982A>G	GRCh38
NC_000002.11:g.73717109A>G , CM000664.1:g.73717109A>G	GRCh37
NC_000002.10:g.73570617A>G	NCBI36
NG_011690.1:g.109230A>G , LRG_741:g.109230A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7642A>G	ENSP00000507671.1:p.Lys2548Glu
ENST00000682801.1:c.7642A>G	ENSP00000507862.1:p.Lys2548Glu
ENST00000682859.1:c.7642A>G	ENSP00000508222.1:p.Lys2548Glu
ENST00000683791.1:c.1034A>G
ENST00000684460.1:c.5094A>G
ENST00000684548.1:c.7642A>G	ENSP00000507421.1:p.Lys2548Glu
ENST00000684590.1:c.2089A>G	ENSP00000507376.1:p.Lys697Glu
ENST00000684656.1:c.5094A>G
ENST00000613296.6:c.8023A>G MANE Select	ENSP00000482968.1:p.Lys2675Glu
ENST00000651434.1:c.896-29793A>G
ENST00000423048.5:c.2854A>G	ENSP00000399833.1:p.Lys952Glu
ENST00000484298.5:c.7897A>G	ENSP00000478155.1:p.Lys2633Glu
ENST00000613296.4:c.8023A>G	ENSP00000482968.1:p.Lys2675Glu
ENST00000614410.4:c.8023A>G	ENSP00000479094.1:p.Lys2675Glu
ENST00000620466.4:n.1826A>G
NM_015120.4:c.8026A>G , LRG_741t1:c.8026A>G	NP_055935.4:p.Lys2676Glu
NM_001378454.1:c.8023A>G MANE Select	NP_001365383.1:p.Lys2675Glu