Canonical Allele Identifier: CA350057844

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009752T>A (hg19) ; chr2:g.206145028T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145028T>A , CM000664.2:g.206145028T>A	GRCh38
NC_000002.11:g.207009752T>A , CM000664.1:g.207009752T>A	GRCh37
NC_000002.10:g.206717997T>A	NCBI36
NG_009248.1:g.19436A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.738-2A>T MANE Select	ENSP00000233190.5:n.738-2A>T
ENST00000233190.10:c.738-2A>T	ENSP00000233190.5:n.738-2A>T
ENST00000423725.5:c.567-2A>T	ENSP00000397760.1:n.567-2A>T
ENST00000432169.5:c.405-2A>T	ENSP00000409689.1:n.405-2A>T
ENST00000440274.5:c.630-2A>T	ENSP00000409766.1:n.630-2A>T
ENST00000449699.5:c.738-2A>T	ENSP00000399912.1:n.738-2A>T
ENST00000455934.6:c.780-2A>T	ENSP00000392709.2:n.780-2A>T
ENST00000457011.5:c.390-2A>T	ENSP00000400976.1:n.390-2A>T
NM_001199981.1:c.630-2A>T	NP_001186910.1:n.630-2A>T
NM_001199982.1:c.405-2A>T	NP_001186911.1:n.405-2A>T
NM_001199983.1:c.567-2A>T	NP_001186912.1:n.567-2A>T
NM_001199984.1:c.780-2A>T	NP_001186913.1:n.780-2A>T
NM_005006.6:c.738-2A>T	NP_004997.4:n.738-2A>T
XM_017004188.2:c.-24A>T	XP_016859677.1:n.-24A>T
NM_001199981.2:c.630-2A>T	NP_001186910.1:n.630-2A>T
NM_001199982.2:c.405-2A>T	NP_001186911.1:n.405-2A>T
NM_001199983.2:c.567-2A>T	NP_001186912.1:n.567-2A>T
NM_005006.7:c.738-2A>T MANE Select	NP_004997.4:n.738-2A>T
NM_001199984.2:c.780-2A>T	NP_001186913.1:n.780-2A>T