Canonical Allele Identifier: CA2184872872

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211862A= , CM000677.2:g.68211862A=	GRCh38
NC_000015.9:g.68504200A= , CM000677.1:g.68504200A=	GRCh37
NC_000015.8:g.66291254A=	NCBI36
NG_008764.2:g.50350T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.299T= MANE Select	ENSP00000249806.5:p.Leu100=
ENST00000562767.2:c.84-14234T=	ENSP00000456336.1:n.84-14234T=
ENST00000563917.2:n.141T=
ENST00000565471.6:c.84-2103T=	ENSP00000457384.1:n.84-2103T=
ENST00000635747.1:c.*202T=	ENSP00000490627.1:n.*202T=
ENST00000636212.1:c.298-121T=	ENSP00000489851.1:n.298-121T=
ENST00000636314.1:c.183-544T=	ENSP00000490295.1:n.183-544T=
ENST00000636674.1:n.1282T=
ENST00000636964.1:n.1471T=
ENST00000637054.1:c.198+6674T=	ENSP00000490807.1:n.198+6674T=
ENST00000637223.1:c.*201-544T=	ENSP00000490010.1:n.*201-544T=
ENST00000637329.1:c.268T=
ENST00000637450.1:c.184T=	ENSP00000490204.1:p.Ser62=
ENST00000637494.1:c.199-544T=	ENSP00000490057.1:n.199-544T=
ENST00000637667.1:c.200T=	ENSP00000489843.1:p.Leu67=
ENST00000637823.1:c.224-219T=
ENST00000637888.1:c.198+6674T=	ENSP00000490546.1:n.198+6674T=
ENST00000638076.1:c.299T=	ENSP00000490373.1:p.Leu100=
ENST00000638144.1:n.130-544T=
ENST00000646164.1:c.38+6674T=
ENST00000249806.9:c.299T=	ENSP00000249806.5:p.Leu100=
ENST00000538696.5:c.395T=	ENSP00000445770.1:p.Leu132=
ENST00000562767.1:c.84-14234T=	ENSP00000456336.1:n.84-14234T=
ENST00000563917.1:n.80T=
ENST00000564752.1:c.299T=	ENSP00000457822.1:p.Leu100=
ENST00000565471.5:c.84-2103T=	ENSP00000457384.1:n.84-2103T=
ENST00000566347.5:c.298-544T=	ENSP00000457783.1:n.298-544T=
ENST00000567060.5:c.298-2142T=	ENSP00000454818.1:n.298-2142T=
NM_017882.2:c.299T=	NP_060352.1:p.Leu100=
XR_931861.1:n.402T=
NM_017882.3:c.299T= MANE Select	NP_060352.1:p.Leu100=