Canonical Allele Identifier: CA347286839

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73800012A>G (hg19) ; chr2:g.73572885A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572885A>G , CM000664.2:g.73572885A>G	GRCh38
NC_000002.11:g.73800012A>G , CM000664.1:g.73800012A>G	GRCh37
NC_000002.10:g.73653520A>G	NCBI36
NG_011690.1:g.192133A>G , LRG_741:g.192133A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10627A>G	ENSP00000507671.1:p.Arg3543Gly
ENST00000682801.1:c.10627A>G	ENSP00000507862.1:p.Arg3543Gly
ENST00000682859.1:c.10627A>G	ENSP00000508222.1:p.Arg3543Gly
ENST00000683791.1:c.3713A>G
ENST00000684460.1:c.7908A>G
ENST00000684548.1:c.10627A>G	ENSP00000507421.1:p.Arg3543Gly
ENST00000684590.1:c.5074A>G	ENSP00000507376.1:p.Arg1692Gly
ENST00000684656.1:c.7953A>G
ENST00000613296.6:c.11008A>G MANE Select	ENSP00000482968.1:p.Arg3670Gly
ENST00000651057.1:c.1162A>G	ENSP00000498504.1:p.Arg388Gly
ENST00000651434.1:c.2364A>G
ENST00000651750.1:c.396A>G
ENST00000652487.1:c.2105A>G
ENST00000423048.5:c.4499A>G	ENSP00000399833.1:n.4499A>G
ENST00000484298.5:c.10882A>G	ENSP00000478155.1:p.Arg3628Gly
ENST00000613296.4:c.11008A>G	ENSP00000482968.1:p.Arg3670Gly
ENST00000614410.4:c.11008A>G	ENSP00000479094.1:p.Arg3670Gly
ENST00000620466.4:n.4811A>G
NM_015120.4:c.11011A>G , LRG_741t1:c.11011A>G	NP_055935.4:p.Arg3671Gly
NM_001378454.1:c.11008A>G MANE Select	NP_001365383.1:p.Arg3670Gly