Canonical Allele Identifier: CA2184876834

Gene: CLN6

Linked Data

• dbSNP Id: rs2093190327
• gnomAD v4: 15-68207528-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68207528A>G , CM000677.2:g.68207528A>G	GRCh38
NC_000015.9:g.68499866A>G , CM000677.1:g.68499866A>G	GRCh37
NC_000015.8:g.66286920A>G	NCBI36
NG_008764.2:g.54684T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.*612T>C MANE Select	ENSP00000249806.5:n.*612T>C
ENST00000562767.2:c.84-9900T>C	ENSP00000456336.1:n.84-9900T>C
ENST00000636964.1:n.3076T>C
ENST00000637054.1:c.199-9900T>C	ENSP00000490807.1:n.199-9900T>C
ENST00000637888.1:c.199-9900T>C	ENSP00000490546.1:n.199-9900T>C
ENST00000638026.1:n.153T>C
ENST00000638076.1:c.*1151T>C	ENSP00000490373.1:n.*1151T>C
ENST00000646164.1:c.39-7847T>C
ENST00000249806.9:c.*612T>C	ENSP00000249806.5:n.*612T>C
ENST00000562767.1:c.84-9900T>C	ENSP00000456336.1:n.84-9900T>C
NM_017882.2:c.*612T>C	NP_060352.1:n.*612T>C
NM_017882.3:c.*612T>C MANE Select	NP_060352.1:n.*612T>C