Canonical Allele Identifier: CA347284143

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73452491C>A , CM000664.2:g.73452491C>A	GRCh38
NC_000002.11:g.73679618C>A , CM000664.1:g.73679618C>A	GRCh37
NC_000002.10:g.73533126C>A	NCBI36
NG_011690.1:g.71739C>A , LRG_741:g.71739C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.5964C>A MANE Select	NP_001365383.1:p.Tyr1988Ter
ENST00000613296.6:c.5964C>A MANE Select	ENSP00000482968.1:p.Tyr1988Ter
NM_015120.4:c.5967C>A , LRG_741t1:c.5967C>A	NP_055935.4:p.Tyr1989Ter
ENST00000423048.5:c.795C>A	ENSP00000399833.1:p.Tyr265Ter
ENST00000484298.5:c.5838C>A	ENSP00000478155.1:p.Tyr1946Ter
ENST00000613296.4:c.5964C>A	ENSP00000482968.1:p.Tyr1988Ter
ENST00000614410.4:c.5964C>A	ENSP00000479094.1:p.Tyr1988Ter
ENST00000682565.1:c.5583C>A	ENSP00000507671.1:p.Tyr1861Ter
ENST00000682801.1:c.5583C>A	ENSP00000507862.1:p.Tyr1861Ter
ENST00000682859.1:c.5583C>A	ENSP00000508222.1:p.Tyr1861Ter
ENST00000683791.1:c.685+20200C>A
ENST00000684197.1:n.933C>A
ENST00000684460.1:c.3035C>A
ENST00000684548.1:c.5583C>A	ENSP00000507421.1:p.Tyr1861Ter
ENST00000684590.1:c.81C>A	ENSP00000507376.1:p.Tyr27Ter
ENST00000684656.1:c.3035C>A