Canonical Allele Identifier: CA347286107

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799911T>A (hg19) ; chr2:g.73572784T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572784T>A , CM000664.2:g.73572784T>A	GRCh38
NC_000002.11:g.73799911T>A , CM000664.1:g.73799911T>A	GRCh37
NC_000002.10:g.73653419T>A	NCBI36
NG_011690.1:g.192032T>A , LRG_741:g.192032T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10526T>A	ENSP00000507671.1:p.Leu3509His
ENST00000682801.1:c.10526T>A	ENSP00000507862.1:p.Leu3509His
ENST00000682859.1:c.10526T>A	ENSP00000508222.1:p.Leu3509His
ENST00000683791.1:c.3612T>A
ENST00000684460.1:c.7807T>A
ENST00000684548.1:c.10526T>A	ENSP00000507421.1:p.Leu3509His
ENST00000684590.1:c.4973T>A	ENSP00000507376.1:p.Leu1658His
ENST00000684656.1:c.7852T>A
ENST00000613296.6:c.10907T>A MANE Select	ENSP00000482968.1:p.Leu3636His
ENST00000651057.1:c.1061T>A	ENSP00000498504.1:p.Leu354His
ENST00000651434.1:c.2263T>A
ENST00000651750.1:c.295T>A
ENST00000652487.1:c.2004T>A
ENST00000423048.5:c.4398T>A	ENSP00000399833.1:n.4398T>A
ENST00000484298.5:c.10781T>A	ENSP00000478155.1:p.Leu3594His
ENST00000613296.4:c.10907T>A	ENSP00000482968.1:p.Leu3636His
ENST00000614410.4:c.10907T>A	ENSP00000479094.1:p.Leu3636His
ENST00000620466.4:n.4710T>A
NM_015120.4:c.10910T>A , LRG_741t1:c.10910T>A	NP_055935.4:p.Leu3637His
NM_001378454.1:c.10907T>A MANE Select	NP_001365383.1:p.Leu3636His