Canonical Allele Identifier: CA2184879101

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209353_68209355delinsCTT , CM000677.2:g.68209353_68209355delinsCTT	GRCh38
NC_000015.9:g.68501691_68501693delinsCTT , CM000677.1:g.68501691_68501693delinsCTT	GRCh37
NC_000015.8:g.66288745_66288747delinsCTT	NCBI36
NG_008764.2:g.52857_52859delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.665+282_665+284delinsAAG MANE Select	ENSP00000249806.5:n.665+282_665+284delinsAAG
ENST00000562767.2:c.84-11727_84-11725delinsAAG	ENSP00000456336.1:n.84-11727_84-11725delinsAAG
ENST00000563917.2:n.507+282_507+284delinsAAG
ENST00000565471.6:c.206+282_206+284delinsAAG	ENSP00000457384.1:n.206+282_206+284delinsAAG
ENST00000635747.1:c.*568+282_*568+284delinsAAG	ENSP00000490627.1:n.*568+282_*568+284delinsAAG
ENST00000636212.1:c.*335+282_*335+284delinsAAG	ENSP00000489851.1:n.*335+282_*335+284delinsAAG
ENST00000636674.1:n.1767+282_1767+284delinsAAG
ENST00000636964.1:n.2193+282_2193+284delinsAAG
ENST00000637054.1:c.198+9181_198+9183delinsAAG	ENSP00000490807.1:n.198+9181_198+9183delinsAAG
ENST00000637329.1:c.634+282_634+284delinsAAG
ENST00000637450.1:c.*319+282_*319+284delinsAAG	ENSP00000490204.1:n.*319+282_*319+284delinsAAG
ENST00000637494.1:c.377+282_377+284delinsAAG	ENSP00000490057.1:n.377+282_377+284delinsAAG
ENST00000637667.1:c.566+282_566+284delinsAAG	ENSP00000489843.1:n.566+282_566+284delinsAAG
ENST00000637823.1:c.490+282_490+284delinsAAG
ENST00000637888.1:c.198+9181_198+9183delinsAAG	ENSP00000490546.1:n.198+9181_198+9183delinsAAG
ENST00000638076.1:c.*268+282_*268+284delinsAAG	ENSP00000490373.1:n.*268+282_*268+284delinsAAG
ENST00000638144.1:n.308+282_308+284delinsAAG
ENST00000646164.1:c.38+9181_38+9183delinsAAG
ENST00000249806.9:c.665+282_665+284delinsAAG	ENSP00000249806.5:n.665+282_665+284delinsAAG
ENST00000538696.5:c.761+282_761+284delinsAAG	ENSP00000445770.1:n.761+282_761+284delinsAAG
ENST00000562767.1:c.84-11727_84-11725delinsAAG	ENSP00000456336.1:n.84-11727_84-11725delinsAAG
ENST00000564752.1:c.*49+282_*49+284delinsAAG	ENSP00000457822.1:n.*49+282_*49+284delinsAAG
ENST00000565471.5:c.206+282_206+284delinsAAG	ENSP00000457384.1:n.206+282_206+284delinsAAG
ENST00000566347.5:c.476+282_476+284delinsAAG	ENSP00000457783.1:n.476+282_476+284delinsAAG
ENST00000567060.5:c.*63+282_*63+284delinsAAG	ENSP00000454818.1:n.*63+282_*63+284delinsAAG
NM_017882.2:c.665+282_665+284delinsAAG	NP_060352.1:n.665+282_665+284delinsAAG
XR_931861.1:n.887+282_887+284delinsAAG
NM_017882.3:c.665+282_665+284delinsAAG MANE Select	NP_060352.1:n.665+282_665+284delinsAAG