Canonical Allele Identifier: CA381536725

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377912T>A (hg19) ; chr11:g.67610441T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610441T>A , CM000673.2:g.67610441T>A	GRCh38
NC_000011.9:g.67377912T>A , CM000673.1:g.67377912T>A	GRCh37
NC_000011.8:g.67134488T>A	NCBI36
NG_013353.1:g.8590T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.571T>A MANE Select	ENSP00000322450.6:p.Tyr191Asn
ENST00000647561.1:c.571T>A	ENSP00000497587.1:p.Tyr191Asn
ENST00000322776.10:c.571T>A	ENSP00000322450.6:p.Tyr191Asn
ENST00000415352.6:c.550T>A	ENSP00000395368.2:p.Tyr184Asn
ENST00000526169.1:n.313T>A
ENST00000526770.5:n.430T>A
ENST00000529867.5:c.535T>A
ENST00000529927.5:c.544T>A	ENSP00000436766.1:p.Tyr182Asn
ENST00000532244.5:c.268T>A	ENSP00000435202.1:p.Tyr90Asn
ENST00000532303.5:c.268T>A	ENSP00000432015.1:p.Tyr90Asn
ENST00000532343.5:c.268T>A	ENSP00000431751.1:p.Tyr90Asn
ENST00000533919.5:c.49T>A	ENSP00000435199.1:p.Tyr17Asn
NM_001166102.1:c.544T>A	NP_001159574.1:p.Tyr182Asn
NM_007103.3:c.571T>A	NP_009034.2:p.Tyr191Asn
NM_001166102.2:c.544T>A	NP_001159574.1:p.Tyr182Asn
NM_007103.4:c.571T>A MANE Select	NP_009034.2:p.Tyr191Asn