Canonical Allele Identifier: CA153862

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144039C>A , CM000664.2:g.206144039C>A	GRCh38
NC_000002.11:g.207008763C>A , CM000664.1:g.207008763C>A	GRCh37
NC_000002.10:g.206717008C>A	NCBI36
NG_009248.1:g.20425G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.966G>T MANE Select	ENSP00000233190.5:p.Ala322=
ENST00000233190.10:c.966G>T	ENSP00000233190.5:p.Ala322=
ENST00000423725.5:c.795G>T	ENSP00000397760.1:p.Ala265=
ENST00000432169.5:c.633G>T	ENSP00000409689.1:p.Ala211=
ENST00000440274.5:c.858G>T	ENSP00000409766.1:p.Ala286=
ENST00000449699.5:c.966G>T	ENSP00000399912.1:p.Ala322=
ENST00000455934.6:c.1008G>T	ENSP00000392709.2:p.Ala336=
ENST00000457011.5:c.618G>T	ENSP00000400976.1:p.Ala206=
NM_001199981.1:c.858G>T	NP_001186910.1:p.Ala286=
NM_001199982.1:c.633G>T	NP_001186911.1:p.Ala211=
NM_001199983.1:c.795G>T	NP_001186912.1:p.Ala265=
NM_001199984.1:c.1008G>T	NP_001186913.1:p.Ala336=
NM_005006.6:c.966G>T	NP_004997.4:p.Ala322=
XM_017004188.2:c.207G>T	XP_016859677.1:p.Ala69=
NM_001199981.2:c.858G>T	NP_001186910.1:p.Ala286=
NM_001199982.2:c.633G>T	NP_001186911.1:p.Ala211=
NM_001199983.2:c.795G>T	NP_001186912.1:p.Ala265=
NM_005006.7:c.966G>T MANE Select	NP_004997.4:p.Ala322=
NM_001199984.2:c.1008G>T	NP_001186913.1:p.Ala336=