Canonical Allele Identifier: CA347278931

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73451153A>T , CM000664.2:g.73451153A>T	GRCh38
NC_000002.11:g.73678280A>T , CM000664.1:g.73678280A>T	GRCh37
NC_000002.10:g.73531788A>T	NCBI36
NG_011690.1:g.70401A>T , LRG_741:g.70401A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.4626A>T MANE Select	NP_001365383.1:p.Gln1542His
ENST00000613296.6:c.4626A>T MANE Select	ENSP00000482968.1:p.Gln1542His
NM_015120.4:c.4629A>T , LRG_741t1:c.4629A>T	NP_055935.4:p.Gln1543His
ENST00000484298.5:c.4500A>T	ENSP00000478155.1:p.Gln1500His
ENST00000613296.4:c.4626A>T	ENSP00000482968.1:p.Gln1542His
ENST00000614410.4:c.4626A>T	ENSP00000479094.1:p.Gln1542His
ENST00000682565.1:c.4245A>T	ENSP00000507671.1:p.Gln1415His
ENST00000682801.1:c.4245A>T	ENSP00000507862.1:p.Gln1415His
ENST00000682859.1:c.4245A>T	ENSP00000508222.1:p.Gln1415His
ENST00000683791.1:c.685+18862A>T
ENST00000684460.1:c.1697A>T
ENST00000684548.1:c.4245A>T	ENSP00000507421.1:p.Gln1415His
ENST00000684656.1:c.1697A>T