Canonical Allele Identifier: CA347283578

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73452381C>T , CM000664.2:g.73452381C>T	GRCh38
NC_000002.11:g.73679508C>T , CM000664.1:g.73679508C>T	GRCh37
NC_000002.10:g.73533016C>T	NCBI36
NG_011690.1:g.71629C>T , LRG_741:g.71629C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.5854C>T MANE Select	NP_001365383.1:p.Gln1952Ter
ENST00000613296.6:c.5854C>T MANE Select	ENSP00000482968.1:p.Gln1952Ter
NM_015120.4:c.5857C>T , LRG_741t1:c.5857C>T	NP_055935.4:p.Gln1953Ter
ENST00000423048.5:c.685C>T	ENSP00000399833.1:p.Gln229Ter
ENST00000484298.5:c.5728C>T	ENSP00000478155.1:p.Gln1910Ter
ENST00000613296.4:c.5854C>T	ENSP00000482968.1:p.Gln1952Ter
ENST00000614410.4:c.5854C>T	ENSP00000479094.1:p.Gln1952Ter
ENST00000682565.1:c.5473C>T	ENSP00000507671.1:p.Gln1825Ter
ENST00000682801.1:c.5473C>T	ENSP00000507862.1:p.Gln1825Ter
ENST00000682859.1:c.5473C>T	ENSP00000508222.1:p.Gln1825Ter
ENST00000683791.1:c.685+20090C>T
ENST00000684197.1:n.823C>T
ENST00000684460.1:c.2925C>T
ENST00000684548.1:c.5473C>T	ENSP00000507421.1:p.Gln1825Ter
ENST00000684656.1:c.2925C>T