Canonical Allele Identifier: CA381569410

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67803832T>A (hg19) ; chr11:g.68036365T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036365T>A , CM000673.2:g.68036365T>A	GRCh38
NC_000011.9:g.67803832T>A , CM000673.1:g.67803832T>A	GRCh37
NC_000011.8:g.67560408T>A	NCBI36
NG_007878.1:g.2350T>A , LRG_115:g.2350T>A
NG_017040.1:g.10749T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.485T>A MANE Select	ENSP00000315774.5:p.Val162Glu
ENST00000313468.9:c.485T>A	ENSP00000315774.5:p.Val162Glu
ENST00000524810.5:c.417T>A
ENST00000526339.5:c.485T>A	ENSP00000436287.1:p.Val162Glu
ENST00000526446.5:c.*540T>A	ENSP00000433645.1:n.*540T>A
ENST00000528492.1:c.47T>A	ENSP00000432848.1:p.Val16Glu
ENST00000531282.1:n.337T>A
NM_002496.3:c.485T>A	NP_002487.1:p.Val162Glu
XM_005274013.1:c.485T>A	XP_005274070.1:p.Val162Glu
XM_005274014.1:c.485T>A	XP_005274071.1:p.Val162Glu
XM_005274015.1:c.365T>A	XP_005274072.1:p.Val122Glu
XM_011545053.1:c.485T>A	XP_011543355.1:p.Val162Glu
NM_002496.4:c.485T>A MANE Select	NP_002487.1:p.Val162Glu