Canonical Allele Identifier: CA347264005

Gene: ALMS1

Linked Data

• dbSNP Id: rs1247701586
• MyVariant Identifiers: chr2:g.73716843G>A (hg19) ; chr2:g.73489716G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489716G>A , CM000664.2:g.73489716G>A	GRCh38
NC_000002.11:g.73716843G>A , CM000664.1:g.73716843G>A	GRCh37
NC_000002.10:g.73570351G>A	NCBI36
NG_011690.1:g.108964G>A , LRG_741:g.108964G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7376G>A	ENSP00000507671.1:p.Cys2459Tyr
ENST00000682801.1:c.7376G>A	ENSP00000507862.1:p.Cys2459Tyr
ENST00000682859.1:c.7376G>A	ENSP00000508222.1:p.Cys2459Tyr
ENST00000683791.1:c.768G>A
ENST00000684460.1:c.4828G>A
ENST00000684548.1:c.7376G>A	ENSP00000507421.1:p.Cys2459Tyr
ENST00000684590.1:c.1823G>A	ENSP00000507376.1:p.Cys608Tyr
ENST00000684656.1:c.4828G>A
ENST00000613296.6:c.7757G>A MANE Select	ENSP00000482968.1:p.Cys2586Tyr
ENST00000651434.1:c.896-30059G>A
ENST00000423048.5:c.2588G>A	ENSP00000399833.1:p.Cys863Tyr
ENST00000484298.5:c.7631G>A	ENSP00000478155.1:p.Cys2544Tyr
ENST00000613296.4:c.7757G>A	ENSP00000482968.1:p.Cys2586Tyr
ENST00000614410.4:c.7757G>A	ENSP00000479094.1:p.Cys2586Tyr
ENST00000620466.4:n.1560G>A
NM_015120.4:c.7760G>A , LRG_741t1:c.7760G>A	NP_055935.4:p.Cys2587Tyr
NM_001378454.1:c.7757G>A MANE Select	NP_001365383.1:p.Cys2586Tyr