Canonical Allele Identifier: CA347286699

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799994A>C (hg19) ; chr2:g.73572867A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572867A>C , CM000664.2:g.73572867A>C	GRCh38
NC_000002.11:g.73799994A>C , CM000664.1:g.73799994A>C	GRCh37
NC_000002.10:g.73653502A>C	NCBI36
NG_011690.1:g.192115A>C , LRG_741:g.192115A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10609A>C	ENSP00000507671.1:p.Ser3537Arg
ENST00000682801.1:c.10609A>C	ENSP00000507862.1:p.Ser3537Arg
ENST00000682859.1:c.10609A>C	ENSP00000508222.1:p.Ser3537Arg
ENST00000683791.1:c.3695A>C
ENST00000684460.1:c.7890A>C
ENST00000684548.1:c.10609A>C	ENSP00000507421.1:p.Ser3537Arg
ENST00000684590.1:c.5056A>C	ENSP00000507376.1:p.Ser1686Arg
ENST00000684656.1:c.7935A>C
ENST00000613296.6:c.10990A>C MANE Select	ENSP00000482968.1:p.Ser3664Arg
ENST00000651057.1:c.1144A>C	ENSP00000498504.1:p.Ser382Arg
ENST00000651434.1:c.2346A>C
ENST00000651750.1:c.378A>C
ENST00000652487.1:c.2087A>C
ENST00000423048.5:c.4481A>C	ENSP00000399833.1:n.4481A>C
ENST00000484298.5:c.10864A>C	ENSP00000478155.1:p.Ser3622Arg
ENST00000613296.4:c.10990A>C	ENSP00000482968.1:p.Ser3664Arg
ENST00000614410.4:c.10990A>C	ENSP00000479094.1:p.Ser3664Arg
ENST00000620466.4:n.4793A>C
NM_015120.4:c.10993A>C , LRG_741t1:c.10993A>C	NP_055935.4:p.Ser3665Arg
NM_001378454.1:c.10990A>C MANE Select	NP_001365383.1:p.Ser3664Arg