Canonical Allele Identifier: CA475417479

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378989G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611518G>C , CM000673.2:g.67611518G>C	GRCh38
NC_000011.9:g.67378989G>C , CM000673.1:g.67378989G>C	GRCh37
NC_000011.8:g.67135565G>C	NCBI36
NG_013353.1:g.9667G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.1029G>C MANE Select	ENSP00000322450.6:p.Val343=
ENST00000647561.1:c.1029G>C	ENSP00000497587.1:p.Val343=
ENST00000322776.10:c.1029G>C	ENSP00000322450.6:p.Val343=
ENST00000415352.6:c.1008G>C	ENSP00000395368.2:p.Val336=
ENST00000526169.1:n.656-4G>C
ENST00000526770.5:n.1312G>C
ENST00000527355.5:c.318G>C	ENSP00000432637.1:p.Val106=
ENST00000527923.1:n.371G>C
ENST00000529927.5:c.1002G>C	ENSP00000436766.1:p.Val334=
ENST00000532303.5:c.726G>C	ENSP00000432015.1:p.Val242=
ENST00000533919.5:c.433G>C	ENSP00000435199.1:n.433G>C
NM_001166102.1:c.1002G>C	NP_001159574.1:p.Val334=
NM_007103.3:c.1029G>C	NP_009034.2:p.Val343=
NM_001166102.2:c.1002G>C	NP_001159574.1:p.Val334=
NM_007103.4:c.1029G>C MANE Select	NP_009034.2:p.Val343=