Canonical Allele Identifier: CA347283644

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799560C>G (hg19) ; chr2:g.73572433C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572433C>G , CM000664.2:g.73572433C>G	GRCh38
NC_000002.11:g.73799560C>G , CM000664.1:g.73799560C>G	GRCh37
NC_000002.10:g.73653068C>G	NCBI36
NG_011690.1:g.191681C>G , LRG_741:g.191681C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10175C>G	ENSP00000507671.1:p.Pro3392Arg
ENST00000682801.1:c.10175C>G	ENSP00000507862.1:p.Pro3392Arg
ENST00000682859.1:c.10175C>G	ENSP00000508222.1:p.Pro3392Arg
ENST00000683791.1:c.3261C>G
ENST00000684460.1:c.7456C>G
ENST00000684548.1:c.10175C>G	ENSP00000507421.1:p.Pro3392Arg
ENST00000684590.1:c.4622C>G	ENSP00000507376.1:p.Pro1541Arg
ENST00000684656.1:c.7501C>G
ENST00000613296.6:c.10556C>G MANE Select	ENSP00000482968.1:p.Pro3519Arg
ENST00000651057.1:c.710C>G	ENSP00000498504.1:p.Pro237Arg
ENST00000651434.1:c.1912C>G
ENST00000652487.1:c.1653C>G
ENST00000423048.5:c.4047C>G	ENSP00000399833.1:n.4047C>G
ENST00000484298.5:c.10430C>G	ENSP00000478155.1:p.Pro3477Arg
ENST00000613296.4:c.10556C>G	ENSP00000482968.1:p.Pro3519Arg
ENST00000614410.4:c.10556C>G	ENSP00000479094.1:p.Pro3519Arg
ENST00000620466.4:n.4359C>G
NM_015120.4:c.10559C>G , LRG_741t1:c.10559C>G	NP_055935.4:p.Pro3520Arg
NM_001378454.1:c.10556C>G MANE Select	NP_001365383.1:p.Pro3519Arg