Canonical Allele Identifier: CA347283503

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799545T>A (hg19) ; chr2:g.73572418T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572418T>A , CM000664.2:g.73572418T>A	GRCh38
NC_000002.11:g.73799545T>A , CM000664.1:g.73799545T>A	GRCh37
NC_000002.10:g.73653053T>A	NCBI36
NG_011690.1:g.191666T>A , LRG_741:g.191666T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10160T>A	ENSP00000507671.1:p.Phe3387Tyr
ENST00000682801.1:c.10160T>A	ENSP00000507862.1:p.Phe3387Tyr
ENST00000682859.1:c.10160T>A	ENSP00000508222.1:p.Phe3387Tyr
ENST00000683791.1:c.3246T>A
ENST00000684460.1:c.7441T>A
ENST00000684548.1:c.10160T>A	ENSP00000507421.1:p.Phe3387Tyr
ENST00000684590.1:c.4607T>A	ENSP00000507376.1:p.Phe1536Tyr
ENST00000684656.1:c.7486T>A
ENST00000613296.6:c.10541T>A MANE Select	ENSP00000482968.1:p.Phe3514Tyr
ENST00000651057.1:c.695T>A	ENSP00000498504.1:p.Phe232Tyr
ENST00000651434.1:c.1897T>A
ENST00000652487.1:c.1638T>A
ENST00000423048.5:c.4032T>A	ENSP00000399833.1:n.4032T>A
ENST00000484298.5:c.10415T>A	ENSP00000478155.1:p.Phe3472Tyr
ENST00000613296.4:c.10541T>A	ENSP00000482968.1:p.Phe3514Tyr
ENST00000614410.4:c.10541T>A	ENSP00000479094.1:p.Phe3514Tyr
ENST00000620466.4:n.4344T>A
NM_015120.4:c.10544T>A , LRG_741t1:c.10544T>A	NP_055935.4:p.Phe3515Tyr
NM_001378454.1:c.10541T>A MANE Select	NP_001365383.1:p.Phe3514Tyr