Canonical Allele Identifier: CA1261020876

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572318A= , CM000664.2:g.73572318A=	GRCh38
NC_000002.11:g.73799445A= , CM000664.1:g.73799445A=	GRCh37
NC_000002.10:g.73652953A=	NCBI36
NG_011690.1:g.191566A= , LRG_741:g.191566A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10060A=	ENSP00000507671.1:p.Lys3354=
ENST00000682801.1:c.10060A=	ENSP00000507862.1:p.Lys3354=
ENST00000682859.1:c.10060A=	ENSP00000508222.1:p.Lys3354=
ENST00000683791.1:c.3146A=
ENST00000684460.1:c.7341A=
ENST00000684548.1:c.10060A=	ENSP00000507421.1:p.Lys3354=
ENST00000684590.1:c.4507A=	ENSP00000507376.1:p.Lys1503=
ENST00000684656.1:c.7386A=
ENST00000613296.6:c.10441A= MANE Select	ENSP00000482968.1:p.Lys3481=
ENST00000651057.1:c.595A=	ENSP00000498504.1:p.Lys199=
ENST00000651434.1:c.1797A=
ENST00000652487.1:c.1538A=
ENST00000423048.5:c.3932A=	ENSP00000399833.1:n.3932A=
ENST00000484298.5:c.10315A=	ENSP00000478155.1:p.Lys3439=
ENST00000613296.4:c.10441A=	ENSP00000482968.1:p.Lys3481=
ENST00000614410.4:c.10441A=	ENSP00000479094.1:p.Lys3481=
ENST00000620466.4:n.4244A=
NM_015120.4:c.10444A= , LRG_741t1:c.10444A=	NP_055935.4:p.Lys3482=
NM_001378454.1:c.10441A= MANE Select	NP_001365383.1:p.Lys3481=