Canonical Allele Identifier: CA1713441

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73449496A>G , CM000664.2:g.73449496A>G	GRCh38
NC_000002.11:g.73676623A>G , CM000664.1:g.73676623A>G	GRCh37
NC_000002.10:g.73530131A>G	NCBI36
NG_011690.1:g.68744A>G , LRG_741:g.68744A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.2969A>G MANE Select	NP_001365383.1:p.Gln990Arg
ENST00000613296.6:c.2969A>G MANE Select	ENSP00000482968.1:p.Gln990Arg
NM_015120.4:c.2972A>G , LRG_741t1:c.2972A>G	NP_055935.4:p.Gln991Arg
ENST00000484298.5:c.2843A>G	ENSP00000478155.1:p.Gln948Arg
ENST00000613296.4:c.2969A>G	ENSP00000482968.1:p.Gln990Arg
ENST00000614410.4:c.2969A>G	ENSP00000479094.1:p.Gln990Arg
ENST00000682565.1:c.2588A>G	ENSP00000507671.1:p.Gln863Arg
ENST00000682801.1:c.2588A>G	ENSP00000507862.1:p.Gln863Arg
ENST00000682859.1:c.2588A>G	ENSP00000508222.1:p.Gln863Arg
ENST00000683791.1:c.685+17205A>G
ENST00000684460.1:c.40A>G
ENST00000684548.1:c.2588A>G	ENSP00000507421.1:p.Gln863Arg
ENST00000684656.1:c.40A>G