Canonical Allele Identifier: CA2629162568

Gene: CLN6

Linked Data

• gnomAD v4: 15-68207898-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68207898C>T , CM000677.2:g.68207898C>T	GRCh38
NC_000015.9:g.68500236C>T , CM000677.1:g.68500236C>T	GRCh37
NC_000015.8:g.66287290C>T	NCBI36
NG_008764.2:g.54314G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.*242G>A MANE Select	ENSP00000249806.5:n.*242G>A
ENST00000562767.2:c.84-10270G>A	ENSP00000456336.1:n.84-10270G>A
ENST00000565471.6:c.*242G>A	ENSP00000457384.1:n.*242G>A
ENST00000636964.1:n.2706G>A
ENST00000637054.1:c.199-10270G>A	ENSP00000490807.1:n.199-10270G>A
ENST00000637329.1:c.1147G>A
ENST00000637888.1:c.199-10270G>A	ENSP00000490546.1:n.199-10270G>A
ENST00000638076.1:c.*781G>A	ENSP00000490373.1:n.*781G>A
ENST00000646164.1:c.39-8217G>A
ENST00000249806.9:c.*242G>A	ENSP00000249806.5:n.*242G>A
ENST00000562767.1:c.84-10270G>A	ENSP00000456336.1:n.84-10270G>A
ENST00000565471.5:c.*242G>A	ENSP00000457384.1:n.*242G>A
NM_017882.2:c.*242G>A	NP_060352.1:n.*242G>A
NM_017882.3:c.*242G>A MANE Select	NP_060352.1:n.*242G>A