Canonical Allele Identifier: CA2662803113

Gene: NDUFS1

Linked Data

• gnomAD v4: 2-206123265-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206123265A>G , CM000664.2:g.206123265A>G	GRCh38
NC_000002.11:g.206987989A>G , CM000664.1:g.206987989A>G	GRCh37
NC_000002.10:g.206696234A>G	NCBI36
NG_009248.1:g.41199T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000233190.11:c.*920T>C MANE Select	ENSP00000233190.5:n.*920T>C
ENST00000233190.10:c.*920T>C	ENSP00000233190.5:n.*920T>C
ENST00000455934.6:c.*920T>C	ENSP00000392709.2:n.*920T>C
NM_001199981.1:c.*920T>C	NP_001186910.1:n.*920T>C
NM_001199982.1:c.*920T>C	NP_001186911.1:n.*920T>C
NM_001199983.1:c.*920T>C	NP_001186912.1:n.*920T>C
NM_001199984.1:c.*920T>C	NP_001186913.1:n.*920T>C
NM_005006.6:c.*920T>C	NP_004997.4:n.*920T>C
NM_001199981.2:c.*920T>C	NP_001186910.1:n.*920T>C
NM_001199982.2:c.*920T>C	NP_001186911.1:n.*920T>C
NM_001199983.2:c.*920T>C	NP_001186912.1:n.*920T>C
NM_005006.7:c.*920T>C MANE Select	NP_004997.4:n.*920T>C
NM_001199984.2:c.*920T>C	NP_001186913.1:n.*920T>C