Canonical Allele Identifier: CA347264093

Gene: ALMS1

Linked Data

• gnomAD v4: 2-73489759-C-A
• MyVariant Identifiers: chr2:g.73716886C>A (hg19) ; chr2:g.73489759C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489759C>A , CM000664.2:g.73489759C>A	GRCh38
NC_000002.11:g.73716886C>A , CM000664.1:g.73716886C>A	GRCh37
NC_000002.10:g.73570394C>A	NCBI36
NG_011690.1:g.109007C>A , LRG_741:g.109007C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7419C>A	ENSP00000507671.1:p.His2473Gln
ENST00000682801.1:c.7419C>A	ENSP00000507862.1:p.His2473Gln
ENST00000682859.1:c.7419C>A	ENSP00000508222.1:p.His2473Gln
ENST00000683791.1:c.811C>A
ENST00000684460.1:c.4871C>A
ENST00000684548.1:c.7419C>A	ENSP00000507421.1:p.His2473Gln
ENST00000684590.1:c.1866C>A	ENSP00000507376.1:p.His622Gln
ENST00000684656.1:c.4871C>A
ENST00000613296.6:c.7800C>A MANE Select	ENSP00000482968.1:p.His2600Gln
ENST00000651434.1:c.896-30016C>A
ENST00000423048.5:c.2631C>A	ENSP00000399833.1:p.His877Gln
ENST00000484298.5:c.7674C>A	ENSP00000478155.1:p.His2558Gln
ENST00000613296.4:c.7800C>A	ENSP00000482968.1:p.His2600Gln
ENST00000614410.4:c.7800C>A	ENSP00000479094.1:p.His2600Gln
ENST00000620466.4:n.1603C>A
NM_015120.4:c.7803C>A , LRG_741t1:c.7803C>A	NP_055935.4:p.His2601Gln
NM_001378454.1:c.7800C>A MANE Select	NP_001365383.1:p.His2600Gln