Canonical Allele Identifier: CA381540503

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378895A>T (hg19) ; chr11:g.67611424A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611424A>T , CM000673.2:g.67611424A>T	GRCh38
NC_000011.9:g.67378895A>T , CM000673.1:g.67378895A>T	GRCh37
NC_000011.8:g.67135471A>T	NCBI36
NG_013353.1:g.9573A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.935A>T MANE Select	ENSP00000322450.6:p.Asp312Val
ENST00000647561.1:c.935A>T	ENSP00000497587.1:p.Asp312Val
ENST00000322776.10:c.935A>T	ENSP00000322450.6:p.Asp312Val
ENST00000415352.6:c.914A>T	ENSP00000395368.2:p.Asp305Val
ENST00000526169.1:n.656-98A>T
ENST00000526770.5:n.1218A>T
ENST00000527355.5:c.224A>T	ENSP00000432637.1:p.Asp75Val
ENST00000527923.1:n.277A>T
ENST00000529927.5:c.908A>T	ENSP00000436766.1:p.Asp303Val
ENST00000532303.5:c.632A>T	ENSP00000432015.1:p.Asp211Val
ENST00000533919.5:c.392-53A>T	ENSP00000435199.1:n.392-53A>T
NM_001166102.1:c.908A>T	NP_001159574.1:p.Asp303Val
NM_007103.3:c.935A>T	NP_009034.2:p.Asp312Val
NM_001166102.2:c.908A>T	NP_001159574.1:p.Asp303Val
NM_007103.4:c.935A>T MANE Select	NP_009034.2:p.Asp312Val