Canonical Allele Identifier: CA350056983

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009636C>A (hg19) ; chr2:g.206144912C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144912C>A , CM000664.2:g.206144912C>A	GRCh38
NC_000002.11:g.207009636C>A , CM000664.1:g.207009636C>A	GRCh37
NC_000002.10:g.206717881C>A	NCBI36
NG_009248.1:g.19552G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000233190.11:c.852G>T MANE Select	ENSP00000233190.5:p.Glu284Asp
ENST00000233190.10:c.852G>T	ENSP00000233190.5:p.Glu284Asp
ENST00000423725.5:c.681G>T	ENSP00000397760.1:p.Glu227Asp
ENST00000432169.5:c.519G>T	ENSP00000409689.1:p.Glu173Asp
ENST00000440274.5:c.744G>T	ENSP00000409766.1:p.Glu248Asp
ENST00000449699.5:c.852G>T	ENSP00000399912.1:p.Glu284Asp
ENST00000455934.6:c.894G>T	ENSP00000392709.2:p.Glu298Asp
ENST00000457011.5:c.504G>T	ENSP00000400976.1:p.Glu168Asp
NM_001199981.1:c.744G>T	NP_001186910.1:p.Glu248Asp
NM_001199982.1:c.519G>T	NP_001186911.1:p.Glu173Asp
NM_001199983.1:c.681G>T	NP_001186912.1:p.Glu227Asp
NM_001199984.1:c.894G>T	NP_001186913.1:p.Glu298Asp
NM_005006.6:c.852G>T	NP_004997.4:p.Glu284Asp
XM_017004188.2:c.93G>T	XP_016859677.1:p.Glu31Asp
NM_001199981.2:c.744G>T	NP_001186910.1:p.Glu248Asp
NM_001199982.2:c.519G>T	NP_001186911.1:p.Glu173Asp
NM_001199983.2:c.681G>T	NP_001186912.1:p.Glu227Asp
NM_005006.7:c.852G>T MANE Select	NP_004997.4:p.Glu284Asp
NM_001199984.2:c.894G>T	NP_001186913.1:p.Glu298Asp