Canonical Allele Identifier: CA1712999

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73424512G>C , CM000664.2:g.73424512G>C	GRCh38
NC_000002.11:g.73651640G>C , CM000664.1:g.73651640G>C	GRCh37
NC_000002.10:g.73505148G>C	NCBI36
NG_011690.1:g.43758G>C , LRG_741:g.43758G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.847G>C MANE Select	NP_001365383.1:p.Glu283Gln
ENST00000613296.6:c.847G>C MANE Select	ENSP00000482968.1:p.Glu283Gln
NM_015120.4:c.850G>C , LRG_741t1:c.850G>C	NP_055935.4:p.Glu284Gln
ENST00000484298.5:c.721G>C	ENSP00000478155.1:p.Glu241Gln
ENST00000613296.4:c.847G>C	ENSP00000482968.1:p.Glu283Gln
ENST00000614410.4:c.847G>C	ENSP00000479094.1:p.Glu283Gln
ENST00000682565.1:c.397G>C	ENSP00000507671.1:p.Glu133Gln
ENST00000682675.1:n.807G>C
ENST00000682801.1:c.397G>C	ENSP00000507862.1:p.Glu133Gln
ENST00000682859.1:c.397G>C	ENSP00000508222.1:p.Glu133Gln
ENST00000682889.1:n.812G>C
ENST00000683791.1:c.201G>C
ENST00000684548.1:c.397G>C	ENSP00000507421.1:p.Glu133Gln