Canonical Allele Identifier: CA2629161958

Gene: CLN6

Linked Data

• gnomAD v4: 15-68207517-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68207517T>G , CM000677.2:g.68207517T>G	GRCh38
NC_000015.9:g.68499855T>G , CM000677.1:g.68499855T>G	GRCh37
NC_000015.8:g.66286909T>G	NCBI36
NG_008764.2:g.54695A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.*623A>C MANE Select	ENSP00000249806.5:n.*623A>C
ENST00000562767.2:c.84-9889A>C	ENSP00000456336.1:n.84-9889A>C
ENST00000636964.1:n.3087A>C
ENST00000637054.1:c.199-9889A>C	ENSP00000490807.1:n.199-9889A>C
ENST00000637888.1:c.199-9889A>C	ENSP00000490546.1:n.199-9889A>C
ENST00000638026.1:n.164A>C
ENST00000638076.1:c.*1162A>C	ENSP00000490373.1:n.*1162A>C
ENST00000646164.1:c.39-7836A>C
ENST00000249806.9:c.*623A>C	ENSP00000249806.5:n.*623A>C
ENST00000562767.1:c.84-9889A>C	ENSP00000456336.1:n.84-9889A>C
NM_017882.2:c.*623A>C	NP_060352.1:n.*623A>C
NM_017882.3:c.*623A>C MANE Select	NP_060352.1:n.*623A>C