Canonical Allele Identifier: CA1260981247

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489994T= , CM000664.2:g.73489994T=	GRCh38
NC_000002.11:g.73717121T= , CM000664.1:g.73717121T=	GRCh37
NC_000002.10:g.73570629T=	NCBI36
NG_011690.1:g.109242T= , LRG_741:g.109242T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7654T=	ENSP00000507671.1:p.Trp2552=
ENST00000682801.1:c.7654T=	ENSP00000507862.1:p.Trp2552=
ENST00000682859.1:c.7654T=	ENSP00000508222.1:p.Trp2552=
ENST00000683791.1:c.1046T=
ENST00000684460.1:c.5106T=
ENST00000684548.1:c.7654T=	ENSP00000507421.1:p.Trp2552=
ENST00000684590.1:c.2101T=	ENSP00000507376.1:p.Trp701=
ENST00000684656.1:c.5106T=
ENST00000613296.6:c.8035T= MANE Select	ENSP00000482968.1:p.Trp2679=
ENST00000651434.1:c.896-29781T=
ENST00000423048.5:c.2866T=	ENSP00000399833.1:p.Trp956=
ENST00000484298.5:c.7909T=	ENSP00000478155.1:p.Trp2637=
ENST00000613296.4:c.8035T=	ENSP00000482968.1:p.Trp2679=
ENST00000614410.4:c.8035T=	ENSP00000479094.1:p.Trp2679=
ENST00000620466.4:n.1838T=
NM_015120.4:c.8038T= , LRG_741t1:c.8038T=	NP_055935.4:p.Trp2680=
NM_001378454.1:c.8035T= MANE Select	NP_001365383.1:p.Trp2679=