Canonical Allele Identifier: CA347266617

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73828484A>G (hg19) ; chr2:g.73601357A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601357A>G , CM000664.2:g.73601357A>G	GRCh38
NC_000002.11:g.73828484A>G , CM000664.1:g.73828484A>G	GRCh37
NC_000002.10:g.73681992A>G	NCBI36
NG_011690.1:g.220605A>G , LRG_741:g.220605A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11654A>G	ENSP00000507671.1:p.Asp3885Gly
ENST00000682801.1:c.11167-828A>G	ENSP00000507862.1:n.11167-828A>G
ENST00000682859.1:c.11654A>G	ENSP00000508222.1:p.Asp3885Gly
ENST00000683791.1:c.4740A>G
ENST00000684460.1:c.8935A>G
ENST00000684548.1:c.11654A>G	ENSP00000507421.1:p.Asp3885Gly
ENST00000684590.1:c.6101A>G	ENSP00000507376.1:p.Asp2034Gly
ENST00000684656.1:c.9119A>G
ENST00000613296.6:c.12035A>G MANE Select	ENSP00000482968.1:p.Asp4012Gly
ENST00000651057.1:c.2189A>G	ENSP00000498504.1:p.Asp730Gly
ENST00000651434.1:c.3391A>G
ENST00000651750.1:c.1260+476A>G
ENST00000652487.1:c.3206A>G
ENST00000464408.3:n.210A>G
ENST00000484298.5:c.11909A>G	ENSP00000478155.1:p.Asp3970Gly
ENST00000613296.4:c.12035A>G	ENSP00000482968.1:p.Asp4012Gly
ENST00000620466.4:n.5838A>G
NM_015120.4:c.12038A>G , LRG_741t1:c.12038A>G	NP_055935.4:p.Asp4013Gly
NM_001378454.1:c.12035A>G MANE Select	NP_001365383.1:p.Asp4012Gly