Canonical Allele Identifier: CA2629164941

Gene: CLN6

Linked Data

• gnomAD v4: 15-68211598-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211603del , CM000677.2:g.68211603del	GRCh38
NC_000015.9:g.68503941del , CM000677.1:g.68503941del	GRCh37
NC_000015.8:g.66290995del	NCBI36
NG_008764.2:g.50613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.486+76del MANE Select	ENSP00000249806.5:n.486+76del
ENST00000562767.2:c.84-13971del	ENSP00000456336.1:n.84-13971del
ENST00000563917.2:n.328+76del
ENST00000565471.6:c.84-1840del	ENSP00000457384.1:n.84-1840del
ENST00000635747.1:c.*389+76del	ENSP00000490627.1:n.*389+76del
ENST00000636212.1:c.*113del	ENSP00000489851.1:n.*113del
ENST00000636314.1:c.183-281del	ENSP00000490295.1:n.183-281del
ENST00000636674.1:n.1545del
ENST00000636964.1:n.1734del
ENST00000637054.1:c.198+6937del	ENSP00000490807.1:n.198+6937del
ENST00000637223.1:c.*201-281del	ENSP00000490010.1:n.*201-281del
ENST00000637329.1:c.455+76del
ENST00000637450.1:c.*140+76del	ENSP00000490204.1:n.*140+76del
ENST00000637494.1:c.199-281del	ENSP00000490057.1:n.199-281del
ENST00000637667.1:c.387+76del	ENSP00000489843.1:n.387+76del
ENST00000637823.1:c.268del
ENST00000637888.1:c.198+6937del	ENSP00000490546.1:n.198+6937del
ENST00000638076.1:c.*46del	ENSP00000490373.1:n.*46del
ENST00000638144.1:n.130-281del
ENST00000646164.1:c.38+6937del
ENST00000249806.9:c.486+76del	ENSP00000249806.5:n.486+76del
ENST00000538696.5:c.582+76del	ENSP00000445770.1:n.582+76del
ENST00000562767.1:c.84-13971del	ENSP00000456336.1:n.84-13971del
ENST00000563917.1:n.343del
ENST00000564752.1:c.512+50del	ENSP00000457822.1:n.512+50del
ENST00000565471.5:c.84-1840del	ENSP00000457384.1:n.84-1840del
ENST00000566347.5:c.298-281del	ENSP00000457783.1:n.298-281del
ENST00000567060.5:c.298-1879del	ENSP00000454818.1:n.298-1879del
NM_017882.2:c.486+76del	NP_060352.1:n.486+76del
XR_931861.1:n.665del
NM_017882.3:c.486+76del MANE Select	NP_060352.1:n.486+76del