Canonical Allele Identifier: CA347286633

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799986A>T (hg19) ; chr2:g.73572859A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572859A>T , CM000664.2:g.73572859A>T	GRCh38
NC_000002.11:g.73799986A>T , CM000664.1:g.73799986A>T	GRCh37
NC_000002.10:g.73653494A>T	NCBI36
NG_011690.1:g.192107A>T , LRG_741:g.192107A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10601A>T	ENSP00000507671.1:p.Lys3534Met
ENST00000682801.1:c.10601A>T	ENSP00000507862.1:p.Lys3534Met
ENST00000682859.1:c.10601A>T	ENSP00000508222.1:p.Lys3534Met
ENST00000683791.1:c.3687A>T
ENST00000684460.1:c.7882A>T
ENST00000684548.1:c.10601A>T	ENSP00000507421.1:p.Lys3534Met
ENST00000684590.1:c.5048A>T	ENSP00000507376.1:p.Lys1683Met
ENST00000684656.1:c.7927A>T
ENST00000613296.6:c.10982A>T MANE Select	ENSP00000482968.1:p.Lys3661Met
ENST00000651057.1:c.1136A>T	ENSP00000498504.1:p.Lys379Met
ENST00000651434.1:c.2338A>T
ENST00000651750.1:c.370A>T
ENST00000652487.1:c.2079A>T
ENST00000423048.5:c.4473A>T	ENSP00000399833.1:n.4473A>T
ENST00000484298.5:c.10856A>T	ENSP00000478155.1:p.Lys3619Met
ENST00000613296.4:c.10982A>T	ENSP00000482968.1:p.Lys3661Met
ENST00000614410.4:c.10982A>T	ENSP00000479094.1:p.Lys3661Met
ENST00000620466.4:n.4785A>T
NM_015120.4:c.10985A>T , LRG_741t1:c.10985A>T	NP_055935.4:p.Lys3662Met
NM_001378454.1:c.10982A>T MANE Select	NP_001365383.1:p.Lys3661Met