Canonical Allele Identifier: CA1261021881

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572759C= , CM000664.2:g.73572759C=	GRCh38
NC_000002.11:g.73799886C= , CM000664.1:g.73799886C=	GRCh37
NC_000002.10:g.73653394C=	NCBI36
NG_011690.1:g.192007C= , LRG_741:g.192007C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10501C=	ENSP00000507671.1:p.Arg3501=
ENST00000682801.1:c.10501C=	ENSP00000507862.1:p.Arg3501=
ENST00000682859.1:c.10501C=	ENSP00000508222.1:p.Arg3501=
ENST00000683791.1:c.3587C=
ENST00000684460.1:c.7782C=
ENST00000684548.1:c.10501C=	ENSP00000507421.1:p.Arg3501=
ENST00000684590.1:c.4948C=	ENSP00000507376.1:p.Arg1650=
ENST00000684656.1:c.7827C=
ENST00000613296.6:c.10882C= MANE Select	ENSP00000482968.1:p.Arg3628=
ENST00000651057.1:c.1036C=	ENSP00000498504.1:p.Arg346=
ENST00000651434.1:c.2238C=
ENST00000651750.1:c.270C=
ENST00000652487.1:c.1979C=
ENST00000423048.5:c.4373C=	ENSP00000399833.1:n.4373C=
ENST00000484298.5:c.10756C=	ENSP00000478155.1:p.Arg3586=
ENST00000613296.4:c.10882C=	ENSP00000482968.1:p.Arg3628=
ENST00000614410.4:c.10882C=	ENSP00000479094.1:p.Arg3628=
ENST00000620466.4:n.4685C=
NM_015120.4:c.10885C= , LRG_741t1:c.10885C=	NP_055935.4:p.Arg3629=
NM_001378454.1:c.10882C= MANE Select	NP_001365383.1:p.Arg3628=