Canonical Allele Identifier: CA314053

Gene: CLN8

Linked Data

• ClinVar Variation Id: 205207
• ClinVar RCV Id: RCV000187142 ; RCV000677331 ; RCV000656837 ; RCV001080578 ; RCV001251946 ; RCV002314707 ; RCV003224205
• dbSNP Id: rs142269885
• ExAC: 8:1719594 A / G
• gnomAD v2: 8-1719594-A-G
• gnomAD v3: 8-1771428-A-G
• gnomAD v4: 8-1771428-A-G
• MyVariant Identifiers: chr8:g.1719594A>G (hg19) ; chr8:g.1771428A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1771428A>G , CM000670.2:g.1771428A>G	GRCh38
NC_000008.10:g.1719594A>G , CM000670.1:g.1719594A>G	GRCh37
NC_000008.9:g.1707001A>G	NCBI36
NG_008656.2:g.20651A>G , LRG_691:g.20651A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331222.6:c.374A>G MANE Select	ENSP00000328182.4:p.Asn125Ser
ENST00000519254.2:c.374A>G	ENSP00000490016.1:p.Asn125Ser
ENST00000520991.3:c.374A>G	ENSP00000487905.2:p.Asn125Ser
ENST00000524258.2:c.374A>G	ENSP00000488898.2:p.Asn125Ser
ENST00000635751.1:c.374A>G	ENSP00000489694.1:p.Asn125Ser
ENST00000635773.1:c.327A>G
ENST00000635855.1:c.374A>G	ENSP00000489726.1:p.Asn125Ser
ENST00000635970.1:c.374A>G	ENSP00000490439.1:p.Asn125Ser
ENST00000636175.1:c.174A>G
ENST00000636934.1:c.374A>G	ENSP00000490218.1:p.Asn125Ser
ENST00000637083.1:c.374A>G	ENSP00000490235.1:p.Asn125Ser
ENST00000637156.1:c.374A>G	ENSP00000490458.1:p.Asn125Ser
ENST00000331222.4:c.374A>G	ENSP00000328182.4:p.Asn125Ser
ENST00000520991.2:c.374A>G	ENSP00000487905.1:p.Asn125Ser
NM_018941.3:c.374A>G , LRG_691t1:c.374A>G	NP_061764.2:p.Asn125Ser
XM_005266021.3:c.374A>G	XP_005266078.1:p.Asn125Ser
XM_005266022.1:c.374A>G	XP_005266079.1:p.Asn125Ser
XM_005266023.1:c.374A>G	XP_005266080.1:p.Asn125Ser
XM_011534745.1:c.374A>G	XP_011533047.1:p.Asn125Ser
XM_011534746.1:c.374A>G	XP_011533048.1:p.Asn125Ser
XM_011534747.1:c.374A>G	XP_011533049.1:p.Asn125Ser
XM_005266021.4:c.374A>G	XP_005266078.1:p.Asn125Ser
XM_011534746.2:c.374A>G	XP_011533048.1:p.Asn125Ser
XM_011534747.2:c.374A>G	XP_011533049.1:p.Asn125Ser
NM_018941.4:c.374A>G MANE Select	NP_061764.2:p.Asn125Ser