Canonical Allele Identifier: CA347282629

Gene: ALMS1

Linked Data

• ClinVar Variation Id: 1724467
• ClinVar RCV Id: RCV002309735
• gnomAD v4: 2-73572279-G-T
• MyVariant Identifiers: chr2:g.73799406G>T (hg19) ; chr2:g.73572279G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572279G>T , CM000664.2:g.73572279G>T	GRCh38
NC_000002.11:g.73799406G>T , CM000664.1:g.73799406G>T	GRCh37
NC_000002.10:g.73652914G>T	NCBI36
NG_011690.1:g.191527G>T , LRG_741:g.191527G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10021G>T	ENSP00000507671.1:p.Glu3341Ter
ENST00000682801.1:c.10021G>T	ENSP00000507862.1:p.Glu3341Ter
ENST00000682859.1:c.10021G>T	ENSP00000508222.1:p.Glu3341Ter
ENST00000683791.1:c.3107G>T
ENST00000684460.1:c.7302G>T
ENST00000684548.1:c.10021G>T	ENSP00000507421.1:p.Glu3341Ter
ENST00000684590.1:c.4468G>T	ENSP00000507376.1:p.Glu1490Ter
ENST00000684656.1:c.7347G>T
ENST00000613296.6:c.10402G>T MANE Select	ENSP00000482968.1:p.Glu3468Ter
ENST00000651057.1:c.556G>T	ENSP00000498504.1:p.Glu186Ter
ENST00000651434.1:c.1758G>T
ENST00000652487.1:c.1499G>T
ENST00000423048.5:c.3893G>T	ENSP00000399833.1:n.3893G>T
ENST00000484298.5:c.10276G>T	ENSP00000478155.1:p.Glu3426Ter
ENST00000613296.4:c.10402G>T	ENSP00000482968.1:p.Glu3468Ter
ENST00000614410.4:c.10402G>T	ENSP00000479094.1:p.Glu3468Ter
ENST00000620466.4:n.4205G>T
NM_015120.4:c.10405G>T , LRG_741t1:c.10405G>T	NP_055935.4:p.Glu3469Ter
NM_001378454.1:c.10402G>T MANE Select	NP_001365383.1:p.Glu3468Ter