Canonical Allele Identifier: CA1757673155

Gene: CLN8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1780363G= , CM000670.2:g.1780363G=	GRCh38
NC_000008.10:g.1728529G= , CM000670.1:g.1728529G=	GRCh37
NC_000008.9:g.1715936G=	NCBI36
NG_008656.2:g.29586G= , LRG_691:g.29586G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331222.6:c.657G= MANE Select	ENSP00000328182.4:p.Trp219=
ENST00000519254.2:c.657G=	ENSP00000490016.1:p.Trp219=
ENST00000520991.3:c.*68G=	ENSP00000487905.2:n.*68G=
ENST00000635751.1:c.657G=	ENSP00000489694.1:p.Trp219=
ENST00000635773.1:c.496+8766G=
ENST00000635855.1:c.543+8766G=	ENSP00000489726.1:n.543+8766G=
ENST00000635970.1:c.657G=	ENSP00000490439.1:p.Trp219=
ENST00000636175.1:c.343+8766G=
ENST00000636934.1:c.543+8766G=	ENSP00000490218.1:n.543+8766G=
ENST00000637083.1:c.657G=	ENSP00000490235.1:p.Trp219=
ENST00000637156.1:c.657G=	ENSP00000490458.1:p.Trp219=
ENST00000331222.4:c.657G=	ENSP00000328182.4:p.Trp219=
ENST00000519254.1:n.176G=
ENST00000523237.1:n.432G=
NM_018941.3:c.657G= , LRG_691t1:c.657G=	NP_061764.2:p.Trp219=
XM_005266021.3:c.657G=	XP_005266078.1:p.Trp219=
XM_005266022.1:c.657G=	XP_005266079.1:p.Trp219=
XM_005266023.1:c.657G=	XP_005266080.1:p.Trp219=
XM_011534745.1:c.657G=	XP_011533047.1:p.Trp219=
XM_011534746.1:c.657G=	XP_011533048.1:p.Trp219=
XM_005266021.4:c.657G=	XP_005266078.1:p.Trp219=
XM_011534746.2:c.657G=	XP_011533048.1:p.Trp219=
NM_018941.4:c.657G= MANE Select	NP_061764.2:p.Trp219=