Canonical Allele Identifier: CA347285081

Gene: ALMS1

Linked Data

• gnomAD v4: 2-73572597-A-G
• MyVariant Identifiers: chr2:g.73799724A>G (hg19) ; chr2:g.73572597A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572597A>G , CM000664.2:g.73572597A>G	GRCh38
NC_000002.11:g.73799724A>G , CM000664.1:g.73799724A>G	GRCh37
NC_000002.10:g.73653232A>G	NCBI36
NG_011690.1:g.191845A>G , LRG_741:g.191845A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10339A>G	ENSP00000507671.1:p.Asn3447Asp
ENST00000682801.1:c.10339A>G	ENSP00000507862.1:p.Asn3447Asp
ENST00000682859.1:c.10339A>G	ENSP00000508222.1:p.Asn3447Asp
ENST00000683791.1:c.3425A>G
ENST00000684460.1:c.7620A>G
ENST00000684548.1:c.10339A>G	ENSP00000507421.1:p.Asn3447Asp
ENST00000684590.1:c.4786A>G	ENSP00000507376.1:p.Asn1596Asp
ENST00000684656.1:c.7665A>G
ENST00000613296.6:c.10720A>G MANE Select	ENSP00000482968.1:p.Asn3574Asp
ENST00000651057.1:c.874A>G	ENSP00000498504.1:p.Asn292Asp
ENST00000651434.1:c.2076A>G
ENST00000651750.1:c.108A>G
ENST00000652487.1:c.1817A>G
ENST00000423048.5:c.4211A>G	ENSP00000399833.1:n.4211A>G
ENST00000484298.5:c.10594A>G	ENSP00000478155.1:p.Asn3532Asp
ENST00000613296.4:c.10720A>G	ENSP00000482968.1:p.Asn3574Asp
ENST00000614410.4:c.10720A>G	ENSP00000479094.1:p.Asn3574Asp
ENST00000620466.4:n.4523A>G
NM_015120.4:c.10723A>G , LRG_741t1:c.10723A>G	NP_055935.4:p.Asn3575Asp
NM_001378454.1:c.10720A>G MANE Select	NP_001365383.1:p.Asn3574Asp