Canonical Allele Identifier: CA381541651

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67379417A>T (hg19) ; chr11:g.67611946A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611946A>T , CM000673.2:g.67611946A>T	GRCh38
NC_000011.9:g.67379417A>T , CM000673.1:g.67379417A>T	GRCh37
NC_000011.8:g.67135993A>T	NCBI36
NG_013353.1:g.10095A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1130A>T MANE Select	ENSP00000322450.6:p.Glu377Val
ENST00000647561.1:c.1130A>T	ENSP00000497587.1:p.Glu377Val
ENST00000322776.10:c.1130A>T	ENSP00000322450.6:p.Glu377Val
ENST00000415352.6:c.1109A>T	ENSP00000395368.2:p.Glu370Val
ENST00000526169.1:n.753A>T
ENST00000526770.5:n.1413A>T
ENST00000527355.5:c.370-174A>T	ENSP00000432637.1:n.370-174A>T
ENST00000527923.1:n.472A>T
ENST00000529927.5:c.1103A>T	ENSP00000436766.1:p.Glu368Val
ENST00000531250.1:n.394A>T
ENST00000532303.5:c.827A>T	ENSP00000432015.1:p.Glu276Val
ENST00000533919.5:c.534A>T	ENSP00000435199.1:n.534A>T
ENST00000534352.1:n.228A>T
NM_001166102.1:c.1103A>T	NP_001159574.1:p.Glu368Val
NM_007103.3:c.1130A>T	NP_009034.2:p.Glu377Val
NM_001166102.2:c.1103A>T	NP_001159574.1:p.Glu368Val
NM_007103.4:c.1130A>T MANE Select	NP_009034.2:p.Glu377Val