Canonical Allele Identifier: CA347264002

Gene: ALMS1

Linked Data

• ClinVar Variation Id: 1328663
• ClinVar RCV Id: RCV001797295
• dbSNP Id: rs1485228491
• MyVariant Identifiers: chr2:g.73716842T>A (hg19) ; chr2:g.73489715T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489715T>A , CM000664.2:g.73489715T>A	GRCh38
NC_000002.11:g.73716842T>A , CM000664.1:g.73716842T>A	GRCh37
NC_000002.10:g.73570350T>A	NCBI36
NG_011690.1:g.108963T>A , LRG_741:g.108963T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7375T>A	ENSP00000507671.1:p.Cys2459Ser
ENST00000682801.1:c.7375T>A	ENSP00000507862.1:p.Cys2459Ser
ENST00000682859.1:c.7375T>A	ENSP00000508222.1:p.Cys2459Ser
ENST00000683791.1:c.767T>A
ENST00000684460.1:c.4827T>A
ENST00000684548.1:c.7375T>A	ENSP00000507421.1:p.Cys2459Ser
ENST00000684590.1:c.1822T>A	ENSP00000507376.1:p.Cys608Ser
ENST00000684656.1:c.4827T>A
ENST00000613296.6:c.7756T>A MANE Select	ENSP00000482968.1:p.Cys2586Ser
ENST00000651434.1:c.896-30060T>A
ENST00000423048.5:c.2587T>A	ENSP00000399833.1:p.Cys863Ser
ENST00000484298.5:c.7630T>A	ENSP00000478155.1:p.Cys2544Ser
ENST00000613296.4:c.7756T>A	ENSP00000482968.1:p.Cys2586Ser
ENST00000614410.4:c.7756T>A	ENSP00000479094.1:p.Cys2586Ser
ENST00000620466.4:n.1559T>A
NM_015120.4:c.7759T>A , LRG_741t1:c.7759T>A	NP_055935.4:p.Cys2587Ser
NM_001378454.1:c.7756T>A MANE Select	NP_001365383.1:p.Cys2586Ser