Canonical Allele Identifier: CA2662800571

Gene: NDUFS1

Linked Data

• gnomAD v4: 2-206127665-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127665T>A , CM000664.2:g.206127665T>A	GRCh38
NC_000002.11:g.206992389T>A , CM000664.1:g.206992389T>A	GRCh37
NC_000002.10:g.206700634T>A	NCBI36
NG_009248.1:g.36799A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1884+132A>T MANE Select	ENSP00000233190.5:n.1884+132A>T
ENST00000233190.10:c.1884+132A>T	ENSP00000233190.5:n.1884+132A>T
ENST00000423725.5:c.1713+132A>T	ENSP00000397760.1:n.1713+132A>T
ENST00000432169.5:c.1551+132A>T	ENSP00000409689.1:n.1551+132A>T
ENST00000440274.5:c.1776+132A>T	ENSP00000409766.1:n.1776+132A>T
ENST00000449699.5:c.1884+132A>T	ENSP00000399912.1:n.1884+132A>T
ENST00000455934.6:c.1926+132A>T	ENSP00000392709.2:n.1926+132A>T
ENST00000457011.5:c.1536+132A>T	ENSP00000400976.1:n.1536+132A>T
ENST00000498520.1:n.488A>T
NM_001199981.1:c.1776+132A>T	NP_001186910.1:n.1776+132A>T
NM_001199982.1:c.1551+132A>T	NP_001186911.1:n.1551+132A>T
NM_001199983.1:c.1713+132A>T	NP_001186912.1:n.1713+132A>T
NM_001199984.1:c.1926+132A>T	NP_001186913.1:n.1926+132A>T
NM_005006.6:c.1884+132A>T	NP_004997.4:n.1884+132A>T
XM_017004188.2:c.1125+132A>T	XP_016859677.1:n.1125+132A>T
NM_001199981.2:c.1776+132A>T	NP_001186910.1:n.1776+132A>T
NM_001199982.2:c.1551+132A>T	NP_001186911.1:n.1551+132A>T
NM_001199983.2:c.1713+132A>T	NP_001186912.1:n.1713+132A>T
NM_005006.7:c.1884+132A>T MANE Select	NP_004997.4:n.1884+132A>T
NM_001199984.2:c.1926+132A>T	NP_001186913.1:n.1926+132A>T