Canonical Allele Identifier: CA350043280

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.206992598C>T (hg19) ; chr2:g.206127874C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127874C>T , CM000664.2:g.206127874C>T	GRCh38
NC_000002.11:g.206992598C>T , CM000664.1:g.206992598C>T	GRCh37
NC_000002.10:g.206700843C>T	NCBI36
NG_009248.1:g.36590G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1807G>A MANE Select	ENSP00000233190.5:p.Ala603Thr
ENST00000233190.10:c.1807G>A	ENSP00000233190.5:p.Ala603Thr
ENST00000423725.5:c.1636G>A	ENSP00000397760.1:p.Ala546Thr
ENST00000432169.5:c.1474G>A	ENSP00000409689.1:p.Ala492Thr
ENST00000440274.5:c.1699G>A	ENSP00000409766.1:p.Ala567Thr
ENST00000449699.5:c.1807G>A	ENSP00000399912.1:p.Ala603Thr
ENST00000455934.6:c.1849G>A	ENSP00000392709.2:p.Ala617Thr
ENST00000457011.5:c.1459G>A	ENSP00000400976.1:p.Ala487Thr
ENST00000498520.1:n.279G>A
NM_001199981.1:c.1699G>A	NP_001186910.1:p.Ala567Thr
NM_001199982.1:c.1474G>A	NP_001186911.1:p.Ala492Thr
NM_001199983.1:c.1636G>A	NP_001186912.1:p.Ala546Thr
NM_001199984.1:c.1849G>A	NP_001186913.1:p.Ala617Thr
NM_005006.6:c.1807G>A	NP_004997.4:p.Ala603Thr
XM_017004188.2:c.1048G>A	XP_016859677.1:p.Ala350Thr
NM_001199981.2:c.1699G>A	NP_001186910.1:p.Ala567Thr
NM_001199982.2:c.1474G>A	NP_001186911.1:p.Ala492Thr
NM_001199983.2:c.1636G>A	NP_001186912.1:p.Ala546Thr
NM_005006.7:c.1807G>A MANE Select	NP_004997.4:p.Ala603Thr
NM_001199984.2:c.1849G>A	NP_001186913.1:p.Ala617Thr