Canonical Allele Identifier: CA430943289

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.206992623A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127899A>T , CM000664.2:g.206127899A>T	GRCh38
NC_000002.11:g.206992623A>T , CM000664.1:g.206992623A>T	GRCh37
NC_000002.10:g.206700868A>T	NCBI36
NG_009248.1:g.36565T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1782T>A MANE Select	ENSP00000233190.5:p.Ala594=
ENST00000233190.10:c.1782T>A	ENSP00000233190.5:p.Ala594=
ENST00000423725.5:c.1611T>A	ENSP00000397760.1:p.Ala537=
ENST00000432169.5:c.1449T>A	ENSP00000409689.1:p.Ala483=
ENST00000440274.5:c.1674T>A	ENSP00000409766.1:p.Ala558=
ENST00000449699.5:c.1782T>A	ENSP00000399912.1:p.Ala594=
ENST00000455934.6:c.1824T>A	ENSP00000392709.2:p.Ala608=
ENST00000457011.5:c.1434T>A	ENSP00000400976.1:p.Ala478=
ENST00000498520.1:n.254T>A
NM_001199981.1:c.1674T>A	NP_001186910.1:p.Ala558=
NM_001199982.1:c.1449T>A	NP_001186911.1:p.Ala483=
NM_001199983.1:c.1611T>A	NP_001186912.1:p.Ala537=
NM_001199984.1:c.1824T>A	NP_001186913.1:p.Ala608=
NM_005006.6:c.1782T>A	NP_004997.4:p.Ala594=
XM_017004188.2:c.1023T>A	XP_016859677.1:p.Ala341=
NM_001199981.2:c.1674T>A	NP_001186910.1:p.Ala558=
NM_001199982.2:c.1449T>A	NP_001186911.1:p.Ala483=
NM_001199983.2:c.1611T>A	NP_001186912.1:p.Ala537=
NM_005006.7:c.1782T>A MANE Select	NP_004997.4:p.Ala594=
NM_001199984.2:c.1824T>A	NP_001186913.1:p.Ala608=