Canonical Allele Identifier: CA381599788

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67800643G>C (hg19) ; chr11:g.68033176G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033176G>C , CM000673.2:g.68033176G>C	GRCh38
NC_000011.9:g.67800643G>C , CM000673.1:g.67800643G>C	GRCh37
NC_000011.8:g.67557219G>C	NCBI36
NG_017040.1:g.7560G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.265G>C MANE Select	ENSP00000315774.5:p.Gly89Arg
ENST00000313468.9:c.265G>C	ENSP00000315774.5:p.Gly89Arg
ENST00000432321.6:n.382G>C
ENST00000453471.6:c.265G>C	ENSP00000403972.2:p.Gly89Arg
ENST00000524810.5:c.36G>C
ENST00000525419.5:c.211G>C	ENSP00000433521.1:p.Gly71Arg
ENST00000525628.1:c.265G>C	ENSP00000432968.1:p.Gly89Arg
ENST00000526339.5:c.265G>C	ENSP00000436287.1:p.Gly89Arg
ENST00000526446.5:c.*320G>C	ENSP00000433645.1:n.*320G>C
ENST00000528492.1:c.-67+2443G>C	ENSP00000432848.1:n.-67+2443G>C
ENST00000529645.1:c.443G>C	ENSP00000431293.1:n.443G>C
ENST00000531228.1:c.*107G>C	ENSP00000433054.1:n.*107G>C
ENST00000532399.1:n.970G>C
NM_002496.3:c.265G>C	NP_002487.1:p.Gly89Arg
XM_005274013.1:c.265G>C	XP_005274070.1:p.Gly89Arg
XM_005274014.1:c.265G>C	XP_005274071.1:p.Gly89Arg
XM_005274015.1:c.145G>C	XP_005274072.1:p.Gly49Arg
XM_011545053.1:c.265G>C	XP_011543355.1:p.Gly89Arg
NM_002496.4:c.265G>C MANE Select	NP_002487.1:p.Gly89Arg