Canonical Allele Identifier: CA1980189487

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610233T= , CM000673.2:g.67610233T=	GRCh38
NC_000011.9:g.67377704T= , CM000673.1:g.67377704T=	GRCh37
NC_000011.8:g.67134280T=	NCBI36
NG_013353.1:g.8382T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.511-148T= MANE Select	ENSP00000322450.6:n.511-148T=
ENST00000647561.1:c.511-148T=	ENSP00000497587.1:n.511-148T=
ENST00000322776.10:c.511-148T=	ENSP00000322450.6:n.511-148T=
ENST00000415352.6:c.490-148T=	ENSP00000395368.2:n.490-148T=
ENST00000524838.5:n.1165T=
ENST00000526169.1:n.253-148T=
ENST00000526770.5:n.370-148T=
ENST00000529867.5:c.475-148T=	ENSP00000434438.1:n.475-148T=
ENST00000529927.5:c.484-148T=	ENSP00000436766.1:n.484-148T=
ENST00000530638.1:c.394-148T=	ENSP00000436936.1:n.394-148T=
ENST00000532244.5:c.208-148T=	ENSP00000435202.1:n.208-148T=
ENST00000532303.5:c.208-148T=	ENSP00000432015.1:n.208-148T=
ENST00000532343.5:c.208-148T=	ENSP00000431751.1:n.208-148T=
ENST00000533075.5:c.490-148T=	ENSP00000437267.1:n.490-148T=
NM_001166102.1:c.484-148T=	NP_001159574.1:n.484-148T=
NM_007103.3:c.511-148T=	NP_009034.2:n.511-148T=
NM_001166102.2:c.484-148T=	NP_001159574.1:n.484-148T=
NM_007103.4:c.511-148T= MANE Select	NP_009034.2:n.511-148T=