Canonical Allele Identifier: CA475443112

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67804042T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036575T>A , CM000673.2:g.68036575T>A	GRCh38
NC_000011.9:g.67804042T>A , CM000673.1:g.67804042T>A	GRCh37
NC_000011.8:g.67560618T>A	NCBI36
NG_007878.1:g.2560T>A , LRG_115:g.2560T>A
NG_017040.1:g.10959T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.615T>A MANE Select	ENSP00000315774.5:p.Ala205=
ENST00000313468.9:c.615T>A	ENSP00000315774.5:p.Ala205=
ENST00000524810.5:c.547T>A
ENST00000528492.1:c.177T>A	ENSP00000432848.1:p.Ala59=
ENST00000531282.1:n.467T>A
NM_002496.3:c.615T>A	NP_002487.1:p.Ala205=
XM_005274013.1:c.615T>A	XP_005274070.1:p.Ala205=
XM_005274014.1:c.615T>A	XP_005274071.1:p.Ala205=
XM_005274015.1:c.495T>A	XP_005274072.1:p.Ala165=
XM_011545053.1:c.615T>A	XP_011543355.1:p.Ala205=
NM_002496.4:c.615T>A MANE Select	NP_002487.1:p.Ala205=