Canonical Allele Identifier: CA2103418172

Gene: CLN5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76992100T= , CM000675.2:g.76992100T=	GRCh38
NC_000013.10:g.77566235T= , CM000675.1:g.77566235T=	GRCh37
NC_000013.9:g.76464236T=	NCBI36
NG_009064.1:g.5177T= , LRG_692:g.5177T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.2T= MANE Select	ENSP00000366673.5:p.Met1=
ENST00000485938.4:c.2T=	ENSP00000482959.3:p.Met1=
ENST00000616833.6:c.2T=	ENSP00000479547.3:p.Met1=
ENST00000635905.1:n.3T=
ENST00000635989.1:n.12T=
ENST00000636183.2:c.2T=	ENSP00000490181.2:p.Met1=
ENST00000636525.2:c.2T=	ENSP00000490078.2:p.Met1=
ENST00000636767.2:c.2T=	ENSP00000489855.2:p.Met1=
ENST00000636780.2:c.2T=	ENSP00000489809.2:p.Met1=
ENST00000637397.2:c.2T=	ENSP00000490422.2:p.Met1=
ENST00000637537.2:c.2T=	ENSP00000489711.2:p.Met1=
ENST00000638147.2:c.2T=	ENSP00000490953.2:p.Met1=
ENST00000377453.7:c.149T=	ENSP00000366673.3:p.Met50=
ENST00000616833.4:c.2T=	ENSP00000479547.1:p.Met1=
NM_006493.2:c.149T= , LRG_692t1:c.149T=	NP_006484.1:p.Met50=
XM_011534917.1:c.149T=	XP_011533219.1:p.Met50=
NM_001366624.1:c.2T=	NP_001353553.1:p.Met1=
NM_006493.3:c.2T=	NP_006484.2:p.Met1=
NM_001366624.2:c.2T=	NP_001353553.1:p.Met1=
NM_006493.4:c.2T= MANE Select	NP_006484.2:p.Met1=