Canonical Allele Identifier: CA381569342

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67803815C>G (hg19) ; chr11:g.68036348C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036348C>G , CM000673.2:g.68036348C>G	GRCh38
NC_000011.9:g.67803815C>G , CM000673.1:g.67803815C>G	GRCh37
NC_000011.8:g.67560391C>G	NCBI36
NG_007878.1:g.2333C>G , LRG_115:g.2333C>G
NG_017040.1:g.10732C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.468C>G MANE Select	ENSP00000315774.5:p.Cys156Trp
ENST00000313468.9:c.468C>G	ENSP00000315774.5:p.Cys156Trp
ENST00000524810.5:c.400C>G
ENST00000525419.5:c.414C>G	ENSP00000433521.1:p.Cys138Trp
ENST00000526339.5:c.468C>G	ENSP00000436287.1:p.Cys156Trp
ENST00000526446.5:c.*523C>G	ENSP00000433645.1:n.*523C>G
ENST00000528492.1:c.30C>G	ENSP00000432848.1:p.Cys10Trp
ENST00000531282.1:n.320C>G
NM_002496.3:c.468C>G	NP_002487.1:p.Cys156Trp
XM_005274013.1:c.468C>G	XP_005274070.1:p.Cys156Trp
XM_005274014.1:c.468C>G	XP_005274071.1:p.Cys156Trp
XM_005274015.1:c.348C>G	XP_005274072.1:p.Cys116Trp
XM_011545053.1:c.468C>G	XP_011543355.1:p.Cys156Trp
NM_002496.4:c.468C>G MANE Select	NP_002487.1:p.Cys156Trp