Canonical Allele Identifier: CA381599776

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67800641A>T (hg19) ; chr11:g.68033174A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033174A>T , CM000673.2:g.68033174A>T	GRCh38
NC_000011.9:g.67800641A>T , CM000673.1:g.67800641A>T	GRCh37
NC_000011.8:g.67557217A>T	NCBI36
NG_017040.1:g.7558A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.263A>T MANE Select	ENSP00000315774.5:p.Lys88Met
ENST00000313468.9:c.263A>T	ENSP00000315774.5:p.Lys88Met
ENST00000432321.6:n.380A>T
ENST00000453471.6:c.263A>T	ENSP00000403972.2:p.Lys88Met
ENST00000524810.5:c.34A>T
ENST00000525419.5:c.209A>T	ENSP00000433521.1:p.Lys70Met
ENST00000525628.1:c.263A>T	ENSP00000432968.1:p.Lys88Met
ENST00000526339.5:c.263A>T	ENSP00000436287.1:p.Lys88Met
ENST00000526446.5:c.*318A>T	ENSP00000433645.1:n.*318A>T
ENST00000528492.1:c.-67+2441A>T	ENSP00000432848.1:n.-67+2441A>T
ENST00000529645.1:c.441A>T	ENSP00000431293.1:n.441A>T
ENST00000531228.1:c.*105A>T	ENSP00000433054.1:n.*105A>T
ENST00000532399.1:n.968A>T
NM_002496.3:c.263A>T	NP_002487.1:p.Lys88Met
XM_005274013.1:c.263A>T	XP_005274070.1:p.Lys88Met
XM_005274014.1:c.263A>T	XP_005274071.1:p.Lys88Met
XM_005274015.1:c.143A>T	XP_005274072.1:p.Lys48Met
XM_011545053.1:c.263A>T	XP_011543355.1:p.Lys88Met
NM_002496.4:c.263A>T MANE Select	NP_002487.1:p.Lys88Met