Canonical Allele Identifier: CA347283199

Gene: ALMS1

Linked Data

• dbSNP Id: rs1674948478
• MyVariant Identifiers: chr2:g.73799496C>T (hg19) ; chr2:g.73572369C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572369C>T , CM000664.2:g.73572369C>T	GRCh38
NC_000002.11:g.73799496C>T , CM000664.1:g.73799496C>T	GRCh37
NC_000002.10:g.73653004C>T	NCBI36
NG_011690.1:g.191617C>T , LRG_741:g.191617C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10111C>T	ENSP00000507671.1:p.His3371Tyr
ENST00000682801.1:c.10111C>T	ENSP00000507862.1:p.His3371Tyr
ENST00000682859.1:c.10111C>T	ENSP00000508222.1:p.His3371Tyr
ENST00000683791.1:c.3197C>T
ENST00000684460.1:c.7392C>T
ENST00000684548.1:c.10111C>T	ENSP00000507421.1:p.His3371Tyr
ENST00000684590.1:c.4558C>T	ENSP00000507376.1:p.His1520Tyr
ENST00000684656.1:c.7437C>T
ENST00000613296.6:c.10492C>T MANE Select	ENSP00000482968.1:p.His3498Tyr
ENST00000651057.1:c.646C>T	ENSP00000498504.1:p.His216Tyr
ENST00000651434.1:c.1848C>T
ENST00000652487.1:c.1589C>T
ENST00000423048.5:c.3983C>T	ENSP00000399833.1:n.3983C>T
ENST00000484298.5:c.10366C>T	ENSP00000478155.1:p.His3456Tyr
ENST00000613296.4:c.10492C>T	ENSP00000482968.1:p.His3498Tyr
ENST00000614410.4:c.10492C>T	ENSP00000479094.1:p.His3498Tyr
ENST00000620466.4:n.4295C>T
NM_015120.4:c.10495C>T , LRG_741t1:c.10495C>T	NP_055935.4:p.His3499Tyr
NM_001378454.1:c.10492C>T MANE Select	NP_001365383.1:p.His3498Tyr