Canonical Allele Identifier: CA381536636

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377894A>C (hg19) ; chr11:g.67610423A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610423A>C , CM000673.2:g.67610423A>C	GRCh38
NC_000011.9:g.67377894A>C , CM000673.1:g.67377894A>C	GRCh37
NC_000011.8:g.67134470A>C	NCBI36
NG_013353.1:g.8572A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.553A>C MANE Select	ENSP00000322450.6:p.Asn185His
ENST00000647561.1:c.553A>C	ENSP00000497587.1:p.Asn185His
ENST00000322776.10:c.553A>C	ENSP00000322450.6:p.Asn185His
ENST00000415352.6:c.532A>C	ENSP00000395368.2:p.Asn178His
ENST00000526169.1:n.295A>C
ENST00000526770.5:n.412A>C
ENST00000529867.5:c.517A>C	ENSP00000434438.1:p.Asn173His
ENST00000529927.5:c.526A>C	ENSP00000436766.1:p.Asn176His
ENST00000532244.5:c.250A>C	ENSP00000435202.1:p.Asn84His
ENST00000532303.5:c.250A>C	ENSP00000432015.1:p.Asn84His
ENST00000532343.5:c.250A>C	ENSP00000431751.1:p.Asn84His
ENST00000533075.5:c.532A>C	ENSP00000437267.1:p.Asn178His
ENST00000533919.5:c.31A>C	ENSP00000435199.1:p.Asn11His
NM_001166102.1:c.526A>C	NP_001159574.1:p.Asn176His
NM_007103.3:c.553A>C	NP_009034.2:p.Asn185His
NM_001166102.2:c.526A>C	NP_001159574.1:p.Asn176His
NM_007103.4:c.553A>C MANE Select	NP_009034.2:p.Asn185His