Canonical Allele Identifier: CA1260981149

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489768T= , CM000664.2:g.73489768T=	GRCh38
NC_000002.11:g.73716895T= , CM000664.1:g.73716895T=	GRCh37
NC_000002.10:g.73570403T=	NCBI36
NG_011690.1:g.109016T= , LRG_741:g.109016T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7428T=	ENSP00000507671.1:p.Ala2476=
ENST00000682801.1:c.7428T=	ENSP00000507862.1:p.Ala2476=
ENST00000682859.1:c.7428T=	ENSP00000508222.1:p.Ala2476=
ENST00000683791.1:c.820T=
ENST00000684460.1:c.4880T=
ENST00000684548.1:c.7428T=	ENSP00000507421.1:p.Ala2476=
ENST00000684590.1:c.1875T=	ENSP00000507376.1:p.Ala625=
ENST00000684656.1:c.4880T=
ENST00000613296.6:c.7809T= MANE Select	ENSP00000482968.1:p.Ala2603=
ENST00000651434.1:c.896-30007T=
ENST00000423048.5:c.2640T=	ENSP00000399833.1:p.Ala880=
ENST00000484298.5:c.7683T=	ENSP00000478155.1:p.Ala2561=
ENST00000613296.4:c.7809T=	ENSP00000482968.1:p.Ala2603=
ENST00000614410.4:c.7809T=	ENSP00000479094.1:p.Ala2603=
ENST00000620466.4:n.1612T=
NM_015120.4:c.7812T= , LRG_741t1:c.7812T=	NP_055935.4:p.Ala2604=
NM_001378454.1:c.7809T= MANE Select	NP_001365383.1:p.Ala2603=