Canonical Allele Identifier: CA361215478

Gene: NDUFA2 TMCO6

Linked Data

• MyVariant Identifiers: chr5:g.140025255G>T (hg19) ; chr5:g.140645670G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140645670G>T , CM000667.2:g.140645670G>T	GRCh38
NC_000005.9:g.140025255G>T , CM000667.1:g.140025255G>T	GRCh37
NC_000005.8:g.140005439G>T	NCBI36
NG_021417.1:g.7116C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252102.9:c.217C>A (NDUFA2) MANE Select	ENSP00000252102.5:p.Gln73Lys
ENST00000252102.8:c.217C>A (NDUFA2)	ENSP00000252102.4:p.Gln73Lys
ENST00000502960.1:n.525C>A (NDUFA2)
ENST00000510680.1:n.59+1586C>A (NDUFA2)
ENST00000512088.1:c.*33C>A (NDUFA2)	ENSP00000427220.1:n.*33C>A
NM_001185012.1:c.*33C>A (NDUFA2)	NP_001171941.1:n.*33C>A
NM_002488.4:c.217C>A (NDUFA2)	NP_002479.1:p.Gln73Lys
NR_033697.1:n.539C>A (NDUFA2)
XM_011537663.1:c.1219-1145G>T (TMCO6)	XP_011535965.1:n.1219-1145G>T
XM_011537663.2:c.1219-1145G>T (TMCO6)	XP_011535965.1:n.1219-1145G>T
NM_002488.5:c.217C>A (NDUFA2) MANE Select	NP_002479.1:p.Gln73Lys
NM_001185012.2:c.*33C>A (NDUFA2)	NP_001171941.1:n.*33C>A
NR_033697.2:n.384C>A (NDUFA2)