Canonical Allele Identifier: CA381536531

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377876G>T (hg19) ; chr11:g.67610405G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610405G>T , CM000673.2:g.67610405G>T	GRCh38
NC_000011.9:g.67377876G>T , CM000673.1:g.67377876G>T	GRCh37
NC_000011.8:g.67134452G>T	NCBI36
NG_013353.1:g.8554G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.535G>T MANE Select	ENSP00000322450.6:p.Ala179Ser
ENST00000647561.1:c.535G>T	ENSP00000497587.1:p.Ala179Ser
ENST00000322776.10:c.535G>T	ENSP00000322450.6:p.Ala179Ser
ENST00000415352.6:c.514G>T	ENSP00000395368.2:p.Ala172Ser
ENST00000526169.1:n.277G>T
ENST00000526770.5:n.394G>T
ENST00000529867.5:c.499G>T	ENSP00000434438.1:p.Ala167Ser
ENST00000529927.5:c.508G>T	ENSP00000436766.1:p.Ala170Ser
ENST00000530638.1:c.418G>T	ENSP00000436936.1:p.Ala140Ser
ENST00000532244.5:c.232G>T	ENSP00000435202.1:p.Ala78Ser
ENST00000532303.5:c.232G>T	ENSP00000432015.1:p.Ala78Ser
ENST00000532343.5:c.232G>T	ENSP00000431751.1:p.Ala78Ser
ENST00000533075.5:c.514G>T	ENSP00000437267.1:p.Ala172Ser
ENST00000533919.5:c.13G>T	ENSP00000435199.1:p.Ala5Ser
NM_001166102.1:c.508G>T	NP_001159574.1:p.Ala170Ser
NM_007103.3:c.535G>T	NP_009034.2:p.Ala179Ser
NM_001166102.2:c.508G>T	NP_001159574.1:p.Ala170Ser
NM_007103.4:c.535G>T MANE Select	NP_009034.2:p.Ala179Ser