Canonical Allele Identifier: CA381599105

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67800420A>G (hg19) ; chr11:g.68032953A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68032953A>G , CM000673.2:g.68032953A>G	GRCh38
NC_000011.9:g.67800420A>G , CM000673.1:g.67800420A>G	GRCh37
NC_000011.8:g.67556996A>G	NCBI36
NG_017040.1:g.7337A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.140A>G MANE Select	ENSP00000315774.5:p.Asp47Gly
ENST00000313468.9:c.140A>G	ENSP00000315774.5:p.Asp47Gly
ENST00000432321.6:n.257A>G
ENST00000453471.6:c.140A>G	ENSP00000403972.2:p.Asp47Gly
ENST00000525419.5:c.86A>G	ENSP00000433521.1:p.Asp29Gly
ENST00000525628.1:c.140A>G	ENSP00000432968.1:p.Asp47Gly
ENST00000526339.5:c.140A>G	ENSP00000436287.1:p.Asp47Gly
ENST00000526446.5:c.*195A>G	ENSP00000433645.1:n.*195A>G
ENST00000528492.1:c.-67+2220A>G	ENSP00000432848.1:n.-67+2220A>G
ENST00000529645.1:c.318A>G	ENSP00000431293.1:n.318A>G
ENST00000531228.1:c.195A>G	ENSP00000433054.1:p.Gly65=
ENST00000532399.1:n.747A>G
NM_002496.3:c.140A>G	NP_002487.1:p.Asp47Gly
XM_005274013.1:c.140A>G	XP_005274070.1:p.Asp47Gly
XM_005274014.1:c.140A>G	XP_005274071.1:p.Asp47Gly
XM_005274015.1:c.20A>G	XP_005274072.1:p.Asp7Gly
XM_011545053.1:c.140A>G	XP_011543355.1:p.Asp47Gly
NM_002496.4:c.140A>G MANE Select	NP_002487.1:p.Asp47Gly