Canonical Allele Identifier: CA475417381

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378974C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611503C>T , CM000673.2:g.67611503C>T	GRCh38
NC_000011.9:g.67378974C>T , CM000673.1:g.67378974C>T	GRCh37
NC_000011.8:g.67135550C>T	NCBI36
NG_013353.1:g.9652C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1014C>T MANE Select	ENSP00000322450.6:p.Asp338=
ENST00000647561.1:c.1014C>T	ENSP00000497587.1:p.Asp338=
ENST00000322776.10:c.1014C>T	ENSP00000322450.6:p.Asp338=
ENST00000415352.6:c.993C>T	ENSP00000395368.2:p.Asp331=
ENST00000526169.1:n.656-19C>T
ENST00000526770.5:n.1297C>T
ENST00000527355.5:c.303C>T	ENSP00000432637.1:p.Asp101=
ENST00000527923.1:n.356C>T
ENST00000529927.5:c.987C>T	ENSP00000436766.1:p.Asp329=
ENST00000532303.5:c.711C>T	ENSP00000432015.1:p.Asp237=
ENST00000533919.5:c.418C>T	ENSP00000435199.1:n.418C>T
NM_001166102.1:c.987C>T	NP_001159574.1:p.Asp329=
NM_007103.3:c.1014C>T	NP_009034.2:p.Asp338=
NM_001166102.2:c.987C>T	NP_001159574.1:p.Asp329=
NM_007103.4:c.1014C>T MANE Select	NP_009034.2:p.Asp338=