Canonical Allele Identifier: CA1714405

Gene: ALMS1

Linked Data

• ClinVar Variation Id: 389822
• ClinVar RCV Id: RCV000443616 ; RCV001833559
• dbSNP Id: rs761272792
• ExAC: 2:73717197 C / T
• gnomAD v2: 2-73717197-C-T
• gnomAD v3: 2-73490070-C-T
• gnomAD v4: 2-73490070-C-T
• MyVariant Identifiers: chr2:g.73717197C>T (hg19) ; chr2:g.73490070C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490070C>T , CM000664.2:g.73490070C>T	GRCh38
NC_000002.11:g.73717197C>T , CM000664.1:g.73717197C>T	GRCh37
NC_000002.10:g.73570705C>T	NCBI36
NG_011690.1:g.109318C>T , LRG_741:g.109318C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7730C>T	ENSP00000507671.1:p.Ser2577Phe
ENST00000682801.1:c.7730C>T	ENSP00000507862.1:p.Ser2577Phe
ENST00000682859.1:c.7730C>T	ENSP00000508222.1:p.Ser2577Phe
ENST00000683791.1:c.1122C>T
ENST00000684460.1:c.5182C>T
ENST00000684548.1:c.7730C>T	ENSP00000507421.1:p.Ser2577Phe
ENST00000684590.1:c.2177C>T	ENSP00000507376.1:p.Ser726Phe
ENST00000684656.1:c.5182C>T
ENST00000613296.6:c.8111C>T MANE Select	ENSP00000482968.1:p.Ser2704Phe
ENST00000651434.1:c.896-29705C>T
ENST00000423048.5:c.2942C>T	ENSP00000399833.1:p.Ser981Phe
ENST00000484298.5:c.7985C>T	ENSP00000478155.1:p.Ser2662Phe
ENST00000613296.4:c.8111C>T	ENSP00000482968.1:p.Ser2704Phe
ENST00000614410.4:c.8111C>T	ENSP00000479094.1:p.Ser2704Phe
ENST00000620466.4:n.1914C>T
NM_015120.4:c.8114C>T , LRG_741t1:c.8114C>T	NP_055935.4:p.Ser2705Phe
NM_001378454.1:c.8111C>T MANE Select	NP_001365383.1:p.Ser2704Phe