Canonical Allele Identifier: CA2184879269

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209466A= , CM000677.2:g.68209466A=	GRCh38
NC_000015.9:g.68501804A= , CM000677.1:g.68501804A=	GRCh37
NC_000015.8:g.66288858A=	NCBI36
NG_008764.2:g.52746T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.665+171T= MANE Select	ENSP00000249806.5:n.665+171T=
ENST00000562767.2:c.84-11838T=	ENSP00000456336.1:n.84-11838T=
ENST00000563917.2:n.507+171T=
ENST00000565471.6:c.206+171T=	ENSP00000457384.1:n.206+171T=
ENST00000635747.1:c.*568+171T=	ENSP00000490627.1:n.*568+171T=
ENST00000636212.1:c.*335+171T=	ENSP00000489851.1:n.*335+171T=
ENST00000636674.1:n.1767+171T=
ENST00000636964.1:n.2193+171T=
ENST00000637054.1:c.198+9070T=	ENSP00000490807.1:n.198+9070T=
ENST00000637329.1:c.634+171T=
ENST00000637450.1:c.*319+171T=	ENSP00000490204.1:n.*319+171T=
ENST00000637494.1:c.377+171T=	ENSP00000490057.1:n.377+171T=
ENST00000637667.1:c.566+171T=	ENSP00000489843.1:n.566+171T=
ENST00000637823.1:c.490+171T=
ENST00000637888.1:c.198+9070T=	ENSP00000490546.1:n.198+9070T=
ENST00000638076.1:c.*268+171T=	ENSP00000490373.1:n.*268+171T=
ENST00000638144.1:n.308+171T=
ENST00000646164.1:c.38+9070T=
ENST00000249806.9:c.665+171T=	ENSP00000249806.5:n.665+171T=
ENST00000538696.5:c.761+171T=	ENSP00000445770.1:n.761+171T=
ENST00000562767.1:c.84-11838T=	ENSP00000456336.1:n.84-11838T=
ENST00000564752.1:c.*49+171T=	ENSP00000457822.1:n.*49+171T=
ENST00000565471.5:c.206+171T=	ENSP00000457384.1:n.206+171T=
ENST00000566347.5:c.476+171T=	ENSP00000457783.1:n.476+171T=
ENST00000567060.5:c.*63+171T=	ENSP00000454818.1:n.*63+171T=
NM_017882.2:c.665+171T=	NP_060352.1:n.665+171T=
XR_931861.1:n.887+171T=
NM_017882.3:c.665+171T= MANE Select	NP_060352.1:n.665+171T=