Canonical Allele Identifier: CA347286978

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73800030A>T (hg19) ; chr2:g.73572903A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572903A>T , CM000664.2:g.73572903A>T	GRCh38
NC_000002.11:g.73800030A>T , CM000664.1:g.73800030A>T	GRCh37
NC_000002.10:g.73653538A>T	NCBI36
NG_011690.1:g.192151A>T , LRG_741:g.192151A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10645A>T	ENSP00000507671.1:p.Lys3549Ter
ENST00000682801.1:c.10645A>T	ENSP00000507862.1:p.Lys3549Ter
ENST00000682859.1:c.10645A>T	ENSP00000508222.1:p.Lys3549Ter
ENST00000683791.1:c.3731A>T
ENST00000684460.1:c.7926A>T
ENST00000684548.1:c.10645A>T	ENSP00000507421.1:p.Lys3549Ter
ENST00000684590.1:c.5092A>T	ENSP00000507376.1:p.Lys1698Ter
ENST00000684656.1:c.7971A>T
ENST00000613296.6:c.11026A>T MANE Select	ENSP00000482968.1:p.Lys3676Ter
ENST00000651057.1:c.1180A>T	ENSP00000498504.1:p.Lys394Ter
ENST00000651434.1:c.2382A>T
ENST00000651750.1:c.414A>T
ENST00000652487.1:c.2123A>T
ENST00000423048.5:c.4517A>T	ENSP00000399833.1:n.4517A>T
ENST00000484298.5:c.10900A>T	ENSP00000478155.1:p.Lys3634Ter
ENST00000613296.4:c.11026A>T	ENSP00000482968.1:p.Lys3676Ter
ENST00000614410.4:c.11026A>T	ENSP00000479094.1:p.Lys3676Ter
ENST00000620466.4:n.4829A>T
NM_015120.4:c.11029A>T , LRG_741t1:c.11029A>T	NP_055935.4:p.Lys3677Ter
NM_001378454.1:c.11026A>T MANE Select	NP_001365383.1:p.Lys3676Ter