Canonical Allele Identifier: CA350042814

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.206992532C>G (hg19) ; chr2:g.206127808C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127808C>G , CM000664.2:g.206127808C>G	GRCh38
NC_000002.11:g.206992532C>G , CM000664.1:g.206992532C>G	GRCh37
NC_000002.10:g.206700777C>G	NCBI36
NG_009248.1:g.36656G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1873G>C MANE Select	ENSP00000233190.5:p.Ala625Pro
ENST00000233190.10:c.1873G>C	ENSP00000233190.5:p.Ala625Pro
ENST00000423725.5:c.1702G>C	ENSP00000397760.1:p.Ala568Pro
ENST00000432169.5:c.1540G>C	ENSP00000409689.1:p.Ala514Pro
ENST00000440274.5:c.1765G>C	ENSP00000409766.1:p.Ala589Pro
ENST00000449699.5:c.1873G>C	ENSP00000399912.1:p.Ala625Pro
ENST00000455934.6:c.1915G>C	ENSP00000392709.2:p.Ala639Pro
ENST00000457011.5:c.1525G>C	ENSP00000400976.1:p.Ala509Pro
ENST00000498520.1:n.345G>C
NM_001199981.1:c.1765G>C	NP_001186910.1:p.Ala589Pro
NM_001199982.1:c.1540G>C	NP_001186911.1:p.Ala514Pro
NM_001199983.1:c.1702G>C	NP_001186912.1:p.Ala568Pro
NM_001199984.1:c.1915G>C	NP_001186913.1:p.Ala639Pro
NM_005006.6:c.1873G>C	NP_004997.4:p.Ala625Pro
XM_017004188.2:c.1114G>C	XP_016859677.1:p.Ala372Pro
NM_001199981.2:c.1765G>C	NP_001186910.1:p.Ala589Pro
NM_001199982.2:c.1540G>C	NP_001186911.1:p.Ala514Pro
NM_001199983.2:c.1702G>C	NP_001186912.1:p.Ala568Pro
NM_005006.7:c.1873G>C MANE Select	NP_004997.4:p.Ala625Pro
NM_001199984.2:c.1915G>C	NP_001186913.1:p.Ala639Pro