Canonical Allele Identifier: CA1714850

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73550379G>A , CM000664.2:g.73550379G>A	GRCh38
NC_000002.11:g.73777506G>A , CM000664.1:g.73777506G>A	GRCh37
NC_000002.10:g.73631014G>A	NCBI36
NG_011690.1:g.169627G>A , LRG_741:g.169627G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.10020G>A MANE Select	NP_001365383.1:p.Arg3340=
ENST00000613296.6:c.10020G>A MANE Select	ENSP00000482968.1:p.Arg3340=
NM_015120.4:c.10023G>A , LRG_741t1:c.10023G>A	NP_055935.4:p.Arg3341=
ENST00000423048.5:c.3511G>A	ENSP00000399833.1:n.3511G>A
ENST00000476650.2:n.199-6841G>A
ENST00000484298.5:c.9894G>A	ENSP00000478155.1:p.Arg3298=
ENST00000613296.4:c.10020G>A	ENSP00000482968.1:p.Arg3340=
ENST00000614410.4:c.10020G>A	ENSP00000479094.1:p.Arg3340=
ENST00000620466.4:n.3823G>A
ENST00000651057.1:c.174G>A	ENSP00000498504.1:p.Arg58=
ENST00000651434.1:c.1376G>A
ENST00000652487.1:c.1117G>A
ENST00000682565.1:c.9639G>A	ENSP00000507671.1:p.Arg3213=
ENST00000682801.1:c.9639G>A	ENSP00000507862.1:p.Arg3213=
ENST00000682859.1:c.9639G>A	ENSP00000508222.1:p.Arg3213=
ENST00000683791.1:c.3031G>A
ENST00000684460.1:c.6979-6841G>A
ENST00000684548.1:c.9639G>A	ENSP00000507421.1:p.Arg3213=
ENST00000684590.1:c.4086G>A	ENSP00000507376.1:p.Arg1362=
ENST00000684656.1:c.6965G>A