Canonical Allele Identifier: CA350043483

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.206992628A>G (hg19) ; chr2:g.206127904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127904A>G , CM000664.2:g.206127904A>G	GRCh38
NC_000002.11:g.206992628A>G , CM000664.1:g.206992628A>G	GRCh37
NC_000002.10:g.206700873A>G	NCBI36
NG_009248.1:g.36560T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1777T>C MANE Select	ENSP00000233190.5:p.Ser593Pro
ENST00000233190.10:c.1777T>C	ENSP00000233190.5:p.Ser593Pro
ENST00000423725.5:c.1606T>C	ENSP00000397760.1:p.Ser536Pro
ENST00000432169.5:c.1444T>C	ENSP00000409689.1:p.Ser482Pro
ENST00000440274.5:c.1669T>C	ENSP00000409766.1:p.Ser557Pro
ENST00000449699.5:c.1777T>C	ENSP00000399912.1:p.Ser593Pro
ENST00000455934.6:c.1819T>C	ENSP00000392709.2:p.Ser607Pro
ENST00000457011.5:c.1429T>C	ENSP00000400976.1:p.Ser477Pro
ENST00000498520.1:n.249T>C
NM_001199981.1:c.1669T>C	NP_001186910.1:p.Ser557Pro
NM_001199982.1:c.1444T>C	NP_001186911.1:p.Ser482Pro
NM_001199983.1:c.1606T>C	NP_001186912.1:p.Ser536Pro
NM_001199984.1:c.1819T>C	NP_001186913.1:p.Ser607Pro
NM_005006.6:c.1777T>C	NP_004997.4:p.Ser593Pro
XM_017004188.2:c.1018T>C	XP_016859677.1:p.Ser340Pro
NM_001199981.2:c.1669T>C	NP_001186910.1:p.Ser557Pro
NM_001199982.2:c.1444T>C	NP_001186911.1:p.Ser482Pro
NM_001199983.2:c.1606T>C	NP_001186912.1:p.Ser536Pro
NM_005006.7:c.1777T>C MANE Select	NP_004997.4:p.Ser593Pro
NM_001199984.2:c.1819T>C	NP_001186913.1:p.Ser607Pro