Canonical Allele Identifier: CA392973552

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504129C>G (hg19) ; chr15:g.68211791C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211791C>G , CM000677.2:g.68211791C>G	GRCh38
NC_000015.9:g.68504129C>G , CM000677.1:g.68504129C>G	GRCh37
NC_000015.8:g.66291183C>G	NCBI36
NG_008764.2:g.50421G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.370G>C MANE Select	ENSP00000249806.5:p.Ala124Pro
ENST00000562767.2:c.84-14163G>C	ENSP00000456336.1:n.84-14163G>C
ENST00000563917.2:n.212G>C
ENST00000565471.6:c.84-2032G>C	ENSP00000457384.1:n.84-2032G>C
ENST00000635747.1:c.*273G>C	ENSP00000490627.1:n.*273G>C
ENST00000636212.1:c.298-50G>C	ENSP00000489851.1:n.298-50G>C
ENST00000636314.1:c.183-473G>C	ENSP00000490295.1:n.183-473G>C
ENST00000636674.1:n.1353G>C
ENST00000636964.1:n.1542G>C
ENST00000637054.1:c.198+6745G>C	ENSP00000490807.1:n.198+6745G>C
ENST00000637223.1:c.*201-473G>C	ENSP00000490010.1:n.*201-473G>C
ENST00000637329.1:c.339G>C
ENST00000637450.1:c.*24G>C	ENSP00000490204.1:n.*24G>C
ENST00000637494.1:c.199-473G>C	ENSP00000490057.1:n.199-473G>C
ENST00000637667.1:c.271G>C	ENSP00000489843.1:p.Ala91Pro
ENST00000637823.1:c.224-148G>C
ENST00000637888.1:c.198+6745G>C	ENSP00000490546.1:n.198+6745G>C
ENST00000638076.1:c.370G>C	ENSP00000490373.1:p.Ala124Pro
ENST00000638144.1:n.130-473G>C
ENST00000646164.1:c.38+6745G>C
ENST00000249806.9:c.370G>C	ENSP00000249806.5:p.Ala124Pro
ENST00000538696.5:c.466G>C	ENSP00000445770.1:p.Ala156Pro
ENST00000562767.1:c.84-14163G>C	ENSP00000456336.1:n.84-14163G>C
ENST00000563917.1:n.151G>C
ENST00000564752.1:c.370G>C	ENSP00000457822.1:p.Ala124Pro
ENST00000565471.5:c.84-2032G>C	ENSP00000457384.1:n.84-2032G>C
ENST00000566347.5:c.298-473G>C	ENSP00000457783.1:n.298-473G>C
ENST00000567060.5:c.298-2071G>C	ENSP00000454818.1:n.298-2071G>C
NM_017882.2:c.370G>C	NP_060352.1:p.Ala124Pro
XR_931861.1:n.473G>C
NM_017882.3:c.370G>C MANE Select	NP_060352.1:p.Ala124Pro