Canonical Allele Identifier: CA2184872228

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211570T= , CM000677.2:g.68211570T=	GRCh38
NC_000015.9:g.68503908T= , CM000677.1:g.68503908T=	GRCh37
NC_000015.8:g.66290962T=	NCBI36
NG_008764.2:g.50642A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.486+105A= MANE Select	ENSP00000249806.5:n.486+105A=
ENST00000562767.2:c.84-13942A=	ENSP00000456336.1:n.84-13942A=
ENST00000563917.2:n.328+105A=
ENST00000565471.6:c.84-1811A=	ENSP00000457384.1:n.84-1811A=
ENST00000635747.1:c.*389+105A=	ENSP00000490627.1:n.*389+105A=
ENST00000636212.1:c.*142A=	ENSP00000489851.1:n.*142A=
ENST00000636314.1:c.183-252A=	ENSP00000490295.1:n.183-252A=
ENST00000636674.1:n.1574A=
ENST00000636964.1:n.1763A=
ENST00000637054.1:c.198+6966A=	ENSP00000490807.1:n.198+6966A=
ENST00000637223.1:c.*201-252A=	ENSP00000490010.1:n.*201-252A=
ENST00000637329.1:c.455+105A=
ENST00000637450.1:c.*140+105A=	ENSP00000490204.1:n.*140+105A=
ENST00000637494.1:c.199-252A=	ENSP00000490057.1:n.199-252A=
ENST00000637667.1:c.387+105A=	ENSP00000489843.1:n.387+105A=
ENST00000637823.1:c.297A=
ENST00000637888.1:c.198+6966A=	ENSP00000490546.1:n.198+6966A=
ENST00000638076.1:c.*75A=	ENSP00000490373.1:n.*75A=
ENST00000638144.1:n.130-252A=
ENST00000646164.1:c.38+6966A=
ENST00000249806.9:c.486+105A=	ENSP00000249806.5:n.486+105A=
ENST00000538696.5:c.582+105A=	ENSP00000445770.1:n.582+105A=
ENST00000562767.1:c.84-13942A=	ENSP00000456336.1:n.84-13942A=
ENST00000563917.1:n.372A=
ENST00000564752.1:c.512+79A=	ENSP00000457822.1:n.512+79A=
ENST00000565471.5:c.84-1811A=	ENSP00000457384.1:n.84-1811A=
ENST00000566347.5:c.298-252A=	ENSP00000457783.1:n.298-252A=
ENST00000567060.5:c.298-1850A=	ENSP00000454818.1:n.298-1850A=
NM_017882.2:c.486+105A=	NP_060352.1:n.486+105A=
XR_931861.1:n.694A=
NM_017882.3:c.486+105A= MANE Select	NP_060352.1:n.486+105A=