Canonical Allele Identifier: CA534125784

Gene: ALMS1

Linked Data

• dbSNP Id: rs1320374
• gnomAD v2: 2-73828310-T-G
• gnomAD v4: 2-73601183-T-G
• MyVariant Identifiers: chr2:g.73828310T>G (hg19) ; chr2:g.73601183T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601183T>G , CM000664.2:g.73601183T>G	GRCh38
NC_000002.11:g.73828310T>G , CM000664.1:g.73828310T>G	GRCh37
NC_000002.10:g.73681818T>G	NCBI36
NG_011690.1:g.220431T>G , LRG_741:g.220431T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11492-12T>G	ENSP00000507671.1:n.11492-12T>G
ENST00000682801.1:c.11167-1002T>G	ENSP00000507862.1:n.11167-1002T>G
ENST00000682859.1:c.11492-12T>G	ENSP00000508222.1:n.11492-12T>G
ENST00000683791.1:c.4578-12T>G
ENST00000684460.1:c.8773-12T>G
ENST00000684548.1:c.11492-12T>G	ENSP00000507421.1:n.11492-12T>G
ENST00000684590.1:c.5939-12T>G	ENSP00000507376.1:n.5939-12T>G
ENST00000684656.1:c.8957-12T>G
ENST00000613296.6:c.11873-12T>G MANE Select	ENSP00000482968.1:n.11873-12T>G
ENST00000651057.1:c.2027-12T>G	ENSP00000498504.1:n.2027-12T>G
ENST00000651434.1:c.3229-12T>G
ENST00000651750.1:c.1260+302T>G
ENST00000652487.1:c.3044-12T>G
ENST00000464408.3:n.48-12T>G
ENST00000484298.5:c.11747-12T>G	ENSP00000478155.1:n.11747-12T>G
ENST00000613296.4:c.11873-12T>G	ENSP00000482968.1:n.11873-12T>G
ENST00000620466.4:n.5676-12T>G
NM_015120.4:c.11876-12T>G , LRG_741t1:c.11876-12T>G	NP_055935.4:n.11876-12T>G
NM_001378454.1:c.11873-12T>G MANE Select	NP_001365383.1:n.11873-12T>G