Canonical Allele Identifier: CA347283632

Gene: ALMS1

Linked Data

• gnomAD v4: 2-73572432-C-G
• MyVariant Identifiers: chr2:g.73799559C>G (hg19) ; chr2:g.73572432C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572432C>G , CM000664.2:g.73572432C>G	GRCh38
NC_000002.11:g.73799559C>G , CM000664.1:g.73799559C>G	GRCh37
NC_000002.10:g.73653067C>G	NCBI36
NG_011690.1:g.191680C>G , LRG_741:g.191680C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10174C>G	ENSP00000507671.1:p.Pro3392Ala
ENST00000682801.1:c.10174C>G	ENSP00000507862.1:p.Pro3392Ala
ENST00000682859.1:c.10174C>G	ENSP00000508222.1:p.Pro3392Ala
ENST00000683791.1:c.3260C>G
ENST00000684460.1:c.7455C>G
ENST00000684548.1:c.10174C>G	ENSP00000507421.1:p.Pro3392Ala
ENST00000684590.1:c.4621C>G	ENSP00000507376.1:p.Pro1541Ala
ENST00000684656.1:c.7500C>G
ENST00000613296.6:c.10555C>G MANE Select	ENSP00000482968.1:p.Pro3519Ala
ENST00000651057.1:c.709C>G	ENSP00000498504.1:p.Pro237Ala
ENST00000651434.1:c.1911C>G
ENST00000652487.1:c.1652C>G
ENST00000423048.5:c.4046C>G	ENSP00000399833.1:n.4046C>G
ENST00000484298.5:c.10429C>G	ENSP00000478155.1:p.Pro3477Ala
ENST00000613296.4:c.10555C>G	ENSP00000482968.1:p.Pro3519Ala
ENST00000614410.4:c.10555C>G	ENSP00000479094.1:p.Pro3519Ala
ENST00000620466.4:n.4358C>G
NM_015120.4:c.10558C>G , LRG_741t1:c.10558C>G	NP_055935.4:p.Pro3520Ala
NM_001378454.1:c.10555C>G MANE Select	NP_001365383.1:p.Pro3519Ala