Canonical Allele Identifier: CA1260981605

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490169C= , CM000664.2:g.73490169C=	GRCh38
NC_000002.11:g.73717296C= , CM000664.1:g.73717296C=	GRCh37
NC_000002.10:g.73570804C=	NCBI36
NG_011690.1:g.109417C= , LRG_741:g.109417C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7829C=	ENSP00000507671.1:p.Thr2610=
ENST00000682801.1:c.7829C=	ENSP00000507862.1:p.Thr2610=
ENST00000682859.1:c.7829C=	ENSP00000508222.1:p.Thr2610=
ENST00000683791.1:c.1221C=
ENST00000684460.1:c.5281C=
ENST00000684548.1:c.7829C=	ENSP00000507421.1:p.Thr2610=
ENST00000684590.1:c.2276C=	ENSP00000507376.1:p.Thr759=
ENST00000684656.1:c.5281C=
ENST00000613296.6:c.8210C= MANE Select	ENSP00000482968.1:p.Thr2737=
ENST00000651434.1:c.896-29606C=
ENST00000423048.5:c.3030+11C=	ENSP00000399833.1:n.3030+11C=
ENST00000484298.5:c.8084C=	ENSP00000478155.1:p.Thr2695=
ENST00000613296.4:c.8210C=	ENSP00000482968.1:p.Thr2737=
ENST00000614410.4:c.8210C=	ENSP00000479094.1:p.Thr2737=
ENST00000620466.4:n.2013C=
NM_015120.4:c.8213C= , LRG_741t1:c.8213C=	NP_055935.4:p.Thr2738=
NM_001378454.1:c.8210C= MANE Select	NP_001365383.1:p.Thr2737=