Canonical Allele Identifier: CA381568851

Gene: NDUFS8

Linked Data

• dbSNP Id: rs1165448240
• MyVariant Identifiers: chr11:g.67803748C>A (hg19) ; chr11:g.68036281C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036281C>A , CM000673.2:g.68036281C>A	GRCh38
NC_000011.9:g.67803748C>A , CM000673.1:g.67803748C>A	GRCh37
NC_000011.8:g.67560324C>A	NCBI36
NG_007878.1:g.2266C>A , LRG_115:g.2266C>A
NG_017040.1:g.10665C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.401C>A MANE Select	ENSP00000315774.5:p.Ala134Asp
ENST00000313468.9:c.401C>A	ENSP00000315774.5:p.Ala134Asp
ENST00000524810.5:c.333C>A
ENST00000525419.5:c.347C>A	ENSP00000433521.1:p.Ala116Asp
ENST00000526339.5:c.401C>A	ENSP00000436287.1:p.Ala134Asp
ENST00000526446.5:c.*456C>A	ENSP00000433645.1:n.*456C>A
ENST00000526542.1:n.352C>A
ENST00000528492.1:c.-38C>A	ENSP00000432848.1:n.-38C>A
ENST00000531282.1:n.253C>A
NM_002496.3:c.401C>A	NP_002487.1:p.Ala134Asp
XM_005274013.1:c.401C>A	XP_005274070.1:p.Ala134Asp
XM_005274014.1:c.401C>A	XP_005274071.1:p.Ala134Asp
XM_005274015.1:c.281C>A	XP_005274072.1:p.Ala94Asp
XM_011545053.1:c.401C>A	XP_011543355.1:p.Ala134Asp
NM_002496.4:c.401C>A MANE Select	NP_002487.1:p.Ala134Asp