Canonical Allele Identifier: CA475417516

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378995A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611524A>G , CM000673.2:g.67611524A>G	GRCh38
NC_000011.9:g.67378995A>G , CM000673.1:g.67378995A>G	GRCh37
NC_000011.8:g.67135571A>G	NCBI36
NG_013353.1:g.9673A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.1035A>G MANE Select	ENSP00000322450.6:p.Ala345=
ENST00000647561.1:c.1035A>G	ENSP00000497587.1:p.Ala345=
ENST00000322776.10:c.1035A>G	ENSP00000322450.6:p.Ala345=
ENST00000415352.6:c.1014A>G	ENSP00000395368.2:p.Ala338=
ENST00000526169.1:n.658A>G
ENST00000526770.5:n.1318A>G
ENST00000527355.5:c.324A>G	ENSP00000432637.1:p.Ala108=
ENST00000527923.1:n.377A>G
ENST00000529927.5:c.1008A>G	ENSP00000436766.1:p.Ala336=
ENST00000532303.5:c.732A>G	ENSP00000432015.1:p.Ala244=
ENST00000533919.5:c.439A>G	ENSP00000435199.1:n.439A>G
NM_001166102.1:c.1008A>G	NP_001159574.1:p.Ala336=
NM_007103.3:c.1035A>G	NP_009034.2:p.Ala345=
NM_001166102.2:c.1008A>G	NP_001159574.1:p.Ala336=
NM_007103.4:c.1035A>G MANE Select	NP_009034.2:p.Ala345=