Canonical Allele Identifier: CA658821970

Gene: ALMS1

Linked Data

• ClinVar Variation Id: 552728
• ClinVar RCV Id: RCV000668045
• dbSNP Id: rs1553409573
• MyVariant Identifiers: chr2:g.73716754C>T (hg19) ; chr2:g.73489627C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489627C>T , CM000664.2:g.73489627C>T	GRCh38
NC_000002.11:g.73716754C>T , CM000664.1:g.73716754C>T	GRCh37
NC_000002.10:g.73570262C>T	NCBI36
NG_011690.1:g.108875C>T , LRG_741:g.108875C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7294-7C>T	ENSP00000507671.1:n.7294-7C>T
ENST00000682801.1:c.7294-7C>T	ENSP00000507862.1:n.7294-7C>T
ENST00000682859.1:c.7294-7C>T	ENSP00000508222.1:n.7294-7C>T
ENST00000683791.1:c.686-7C>T
ENST00000684460.1:c.4746-7C>T
ENST00000684548.1:c.7294-7C>T	ENSP00000507421.1:n.7294-7C>T
ENST00000684590.1:c.1741-7C>T	ENSP00000507376.1:n.1741-7C>T
ENST00000684656.1:c.4746-7C>T
ENST00000613296.6:c.7675-7C>T MANE Select	ENSP00000482968.1:n.7675-7C>T
ENST00000651434.1:c.896-30148C>T
ENST00000423048.5:c.2506-7C>T	ENSP00000399833.1:n.2506-7C>T
ENST00000484298.5:c.7549-7C>T	ENSP00000478155.1:n.7549-7C>T
ENST00000613296.4:c.7675-7C>T	ENSP00000482968.1:n.7675-7C>T
ENST00000614410.4:c.7675-7C>T	ENSP00000479094.1:n.7675-7C>T
ENST00000620466.4:n.1478-7C>T
NM_015120.4:c.7678-7C>T , LRG_741t1:c.7678-7C>T	NP_055935.4:n.7678-7C>T
NM_001378454.1:c.7675-7C>T MANE Select	NP_001365383.1:n.7675-7C>T