Canonical Allele Identifier: CA2103418182

Gene: CLN5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76992103C= , CM000675.2:g.76992103C=	GRCh38
NC_000013.10:g.77566238C= , CM000675.1:g.77566238C=	GRCh37
NC_000013.9:g.76464239C=	NCBI36
NG_009064.1:g.5180C= , LRG_692:g.5180C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.5C= MANE Select	ENSP00000366673.5:p.Ala2=
ENST00000485938.4:c.5C=	ENSP00000482959.3:p.Ala2=
ENST00000616833.6:c.5C=	ENSP00000479547.3:p.Ala2=
ENST00000635905.1:n.6C=
ENST00000635989.1:n.15C=
ENST00000636183.2:c.5C=	ENSP00000490181.2:p.Ala2=
ENST00000636525.2:c.5C=	ENSP00000490078.2:p.Ala2=
ENST00000636767.2:c.5C=	ENSP00000489855.2:p.Ala2=
ENST00000636780.2:c.5C=	ENSP00000489809.2:p.Ala2=
ENST00000637397.2:c.5C=	ENSP00000490422.2:p.Ala2=
ENST00000637537.2:c.5C=	ENSP00000489711.2:p.Ala2=
ENST00000638147.2:c.5C=	ENSP00000490953.2:p.Ala2=
ENST00000377453.7:c.152C=	ENSP00000366673.3:p.Ala51=
ENST00000616833.4:c.5C=	ENSP00000479547.1:p.Ala2=
NM_006493.2:c.152C= , LRG_692t1:c.152C=	NP_006484.1:p.Ala51=
XM_011534917.1:c.152C=	XP_011533219.1:p.Ala51=
NM_001366624.1:c.5C=	NP_001353553.1:p.Ala2=
NM_006493.3:c.5C=	NP_006484.2:p.Ala2=
NM_001366624.2:c.5C=	NP_001353553.1:p.Ala2=
NM_006493.4:c.5C= MANE Select	NP_006484.2:p.Ala2=