Canonical Allele Identifier: CA1261020881

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572320G= , CM000664.2:g.73572320G=	GRCh38
NC_000002.11:g.73799447G= , CM000664.1:g.73799447G=	GRCh37
NC_000002.10:g.73652955G=	NCBI36
NG_011690.1:g.191568G= , LRG_741:g.191568G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10062G=	ENSP00000507671.1:p.Lys3354=
ENST00000682801.1:c.10062G=	ENSP00000507862.1:p.Lys3354=
ENST00000682859.1:c.10062G=	ENSP00000508222.1:p.Lys3354=
ENST00000683791.1:c.3148G=
ENST00000684460.1:c.7343G=
ENST00000684548.1:c.10062G=	ENSP00000507421.1:p.Lys3354=
ENST00000684590.1:c.4509G=	ENSP00000507376.1:p.Lys1503=
ENST00000684656.1:c.7388G=
ENST00000613296.6:c.10443G= MANE Select	ENSP00000482968.1:p.Lys3481=
ENST00000651057.1:c.597G=	ENSP00000498504.1:p.Lys199=
ENST00000651434.1:c.1799G=
ENST00000652487.1:c.1540G=
ENST00000423048.5:c.3934G=	ENSP00000399833.1:n.3934G=
ENST00000484298.5:c.10317G=	ENSP00000478155.1:p.Lys3439=
ENST00000613296.4:c.10443G=	ENSP00000482968.1:p.Lys3481=
ENST00000614410.4:c.10443G=	ENSP00000479094.1:p.Lys3481=
ENST00000620466.4:n.4246G=
NM_015120.4:c.10446G= , LRG_741t1:c.10446G=	NP_055935.4:p.Lys3482=
NM_001378454.1:c.10443G= MANE Select	NP_001365383.1:p.Lys3481=