Canonical Allele Identifier: CA381599094

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67800418G>C (hg19) ; chr11:g.68032951G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68032951G>C , CM000673.2:g.68032951G>C	GRCh38
NC_000011.9:g.67800418G>C , CM000673.1:g.67800418G>C	GRCh37
NC_000011.8:g.67556994G>C	NCBI36
NG_017040.1:g.7335G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.138G>C MANE Select	ENSP00000315774.5:p.Met46Ile
ENST00000313468.9:c.138G>C	ENSP00000315774.5:p.Met46Ile
ENST00000432321.6:n.255G>C
ENST00000453471.6:c.138G>C	ENSP00000403972.2:p.Met46Ile
ENST00000525419.5:c.84G>C	ENSP00000433521.1:p.Met28Ile
ENST00000525628.1:c.138G>C	ENSP00000432968.1:p.Met46Ile
ENST00000526339.5:c.138G>C	ENSP00000436287.1:p.Met46Ile
ENST00000526446.5:c.*193G>C	ENSP00000433645.1:n.*193G>C
ENST00000528492.1:c.-67+2218G>C	ENSP00000432848.1:n.-67+2218G>C
ENST00000529645.1:c.316G>C	ENSP00000431293.1:n.316G>C
ENST00000531228.1:c.193G>C	ENSP00000433054.1:p.Gly65Arg
ENST00000532399.1:n.745G>C
NM_002496.3:c.138G>C	NP_002487.1:p.Met46Ile
XM_005274013.1:c.138G>C	XP_005274070.1:p.Met46Ile
XM_005274014.1:c.138G>C	XP_005274071.1:p.Met46Ile
XM_005274015.1:c.18G>C	XP_005274072.1:p.Met6Ile
XM_011545053.1:c.138G>C	XP_011543355.1:p.Met46Ile
NM_002496.4:c.138G>C MANE Select	NP_002487.1:p.Met46Ile