Canonical Allele Identifier: CA2184879915

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209925G= , CM000677.2:g.68209925G=	GRCh38
NC_000015.9:g.68502263G= , CM000677.1:g.68502263G=	GRCh37
NC_000015.8:g.66289317G=	NCBI36
NG_008764.2:g.52287C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.543-166C= MANE Select	ENSP00000249806.5:n.543-166C=
ENST00000562767.2:c.84-12297C=	ENSP00000456336.1:n.84-12297C=
ENST00000563917.2:n.385-166C=
ENST00000565471.6:c.84-166C=	ENSP00000457384.1:n.84-166C=
ENST00000635747.1:c.*446-166C=	ENSP00000490627.1:n.*446-166C=
ENST00000636212.1:c.*213-166C=	ENSP00000489851.1:n.*213-166C=
ENST00000636314.1:c.239-166C=	ENSP00000490295.1:n.239-166C=
ENST00000636674.1:n.1645-166C=
ENST00000636964.1:n.2071-166C=
ENST00000637054.1:c.198+8611C=	ENSP00000490807.1:n.198+8611C=
ENST00000637223.1:c.*257-166C=	ENSP00000490010.1:n.*257-166C=
ENST00000637329.1:c.512-166C=
ENST00000637450.1:c.*197-166C=	ENSP00000490204.1:n.*197-166C=
ENST00000637494.1:c.255-166C=	ENSP00000490057.1:n.255-166C=
ENST00000637667.1:c.444-166C=	ENSP00000489843.1:n.444-166C=
ENST00000637823.1:c.368-166C=
ENST00000637888.1:c.198+8611C=	ENSP00000490546.1:n.198+8611C=
ENST00000638076.1:c.*146-166C=	ENSP00000490373.1:n.*146-166C=
ENST00000638144.1:n.186-166C=
ENST00000646164.1:c.38+8611C=
ENST00000249806.9:c.543-166C=	ENSP00000249806.5:n.543-166C=
ENST00000538696.5:c.639-166C=	ENSP00000445770.1:n.639-166C=
ENST00000562767.1:c.84-12297C=	ENSP00000456336.1:n.84-12297C=
ENST00000563917.1:n.443-166C=
ENST00000564752.1:c.569-166C=	ENSP00000457822.1:n.569-166C=
ENST00000565471.5:c.84-166C=	ENSP00000457384.1:n.84-166C=
ENST00000566347.5:c.354-166C=	ENSP00000457783.1:n.354-166C=
ENST00000567060.5:c.298-205C=	ENSP00000454818.1:n.298-205C=
NM_017882.2:c.543-166C=	NP_060352.1:n.543-166C=
XR_931861.1:n.765-166C=
NM_017882.3:c.543-166C= MANE Select	NP_060352.1:n.543-166C=