Canonical Allele Identifier: CA388306177

Gene: CLN5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76992096C>A , CM000675.2:g.76992096C>A	GRCh38
NC_000013.10:g.77566231C>A , CM000675.1:g.77566231C>A	GRCh37
NC_000013.9:g.76464232C>A	NCBI36
NG_009064.1:g.5173C>A , LRG_692:g.5173C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.-3C>A MANE Select	ENSP00000366673.5:n.-3C>A
ENST00000485938.4:c.-3C>A	ENSP00000482959.3:n.-3C>A
ENST00000616833.6:c.-3C>A	ENSP00000479547.3:n.-3C>A
ENST00000635989.1:n.8C>A
ENST00000636183.2:c.-3C>A	ENSP00000490181.2:n.-3C>A
ENST00000636525.2:c.-3C>A	ENSP00000490078.2:n.-3C>A
ENST00000636780.2:c.-3C>A	ENSP00000489809.2:n.-3C>A
ENST00000637397.2:c.-3C>A	ENSP00000490422.2:n.-3C>A
ENST00000637537.2:c.-3C>A	ENSP00000489711.2:n.-3C>A
ENST00000638147.2:c.-3C>A	ENSP00000490953.2:n.-3C>A
ENST00000377453.7:c.145C>A	ENSP00000366673.3:p.Leu49Met
ENST00000616833.4:c.-3C>A	ENSP00000479547.1:n.-3C>A
NM_006493.2:c.145C>A , LRG_692t1:c.145C>A	NP_006484.1:p.Leu49Met
XM_011534917.1:c.145C>A	XP_011533219.1:p.Leu49Met
NM_001366624.1:c.-3C>A	NP_001353553.1:n.-3C>A
NM_006493.3:c.-3C>A	NP_006484.2:n.-3C>A
NM_001366624.2:c.-3C>A	NP_001353553.1:n.-3C>A
NM_006493.4:c.-3C>A MANE Select	NP_006484.2:n.-3C>A