Canonical Allele Identifier: CA1261021201

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572447G= , CM000664.2:g.73572447G=	GRCh38
NC_000002.11:g.73799574G= , CM000664.1:g.73799574G=	GRCh37
NC_000002.10:g.73653082G=	NCBI36
NG_011690.1:g.191695G= , LRG_741:g.191695G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10189G=	ENSP00000507671.1:p.Glu3397=
ENST00000682801.1:c.10189G=	ENSP00000507862.1:p.Glu3397=
ENST00000682859.1:c.10189G=	ENSP00000508222.1:p.Glu3397=
ENST00000683791.1:c.3275G=
ENST00000684460.1:c.7470G=
ENST00000684548.1:c.10189G=	ENSP00000507421.1:p.Glu3397=
ENST00000684590.1:c.4636G=	ENSP00000507376.1:p.Glu1546=
ENST00000684656.1:c.7515G=
ENST00000613296.6:c.10570G= MANE Select	ENSP00000482968.1:p.Glu3524=
ENST00000651057.1:c.724G=	ENSP00000498504.1:p.Glu242=
ENST00000651434.1:c.1926G=
ENST00000652487.1:c.1667G=
ENST00000423048.5:c.4061G=	ENSP00000399833.1:n.4061G=
ENST00000484298.5:c.10444G=	ENSP00000478155.1:p.Glu3482=
ENST00000613296.4:c.10570G=	ENSP00000482968.1:p.Glu3524=
ENST00000614410.4:c.10570G=	ENSP00000479094.1:p.Glu3524=
ENST00000620466.4:n.4373G=
NM_015120.4:c.10573G= , LRG_741t1:c.10573G=	NP_055935.4:p.Glu3525=
NM_001378454.1:c.10570G= MANE Select	NP_001365383.1:p.Glu3524=