Canonical Allele Identifier: CA381569244
Gene: NDUFS8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68036332T>C , CM000673.2:g.68036332T>C GRCh38
NC_000011.9:g.67803799T>C , CM000673.1:g.67803799T>C GRCh37
NC_000011.8:g.67560375T>C NCBI36
NG_007878.1:g.2317T>C , LRG_115:g.2317T>C
NG_017040.1:g.10716T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.452T>C MANE Select ENSP00000315774.5:p.Ile151Thr
ENST00000313468.9:c.452T>C ENSP00000315774.5:p.Ile151Thr
ENST00000524810.5:c.384T>C
ENST00000525419.5:c.398T>C ENSP00000433521.1:p.Ile133Thr
ENST00000526339.5:c.452T>C ENSP00000436287.1:p.Ile151Thr
ENST00000526446.5:c.*507T>C ENSP00000433645.1:n.*507T>C
ENST00000528492.1:c.14T>C ENSP00000432848.1:p.Ile5Thr
ENST00000531282.1:n.304T>C
NM_002496.3:c.452T>C NP_002487.1:p.Ile151Thr
XM_005274013.1:c.452T>C XP_005274070.1:p.Ile151Thr
XM_005274014.1:c.452T>C XP_005274071.1:p.Ile151Thr
XM_005274015.1:c.332T>C XP_005274072.1:p.Ile111Thr
XM_011545053.1:c.452T>C XP_011543355.1:p.Ile151Thr
NM_002496.4:c.452T>C MANE Select NP_002487.1:p.Ile151Thr