Canonical Allele Identifier: CA446629120

Gene: NDUFA2 IK

Linked Data

• MyVariant Identifiers: chr5:g.140027127C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140647542C>T , CM000667.2:g.140647542C>T	GRCh38
NC_000005.9:g.140027127C>T , CM000667.1:g.140027127C>T	GRCh37
NC_000005.8:g.140007311C>T	NCBI36
NG_021417.1:g.5244G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252102.9:c.42G>A (NDUFA2) MANE Select	ENSP00000252102.5:p.Leu14=
ENST00000252102.8:c.42G>A (NDUFA2)	ENSP00000252102.4:p.Leu14=
ENST00000502960.1:n.230G>A (NDUFA2)
ENST00000512088.1:c.42G>A (NDUFA2)	ENSP00000427220.1:p.Leu14=
ENST00000513256.5:c.4+233C>T (IK)	ENSP00000425564.1:n.4+233C>T
NM_001185012.1:c.42G>A (NDUFA2)	NP_001171941.1:p.Leu14=
NM_002488.4:c.42G>A (NDUFA2)	NP_002479.1:p.Leu14=
NR_033697.1:n.244G>A (NDUFA2)
NM_002488.5:c.42G>A (NDUFA2) MANE Select	NP_002479.1:p.Leu14=
NM_001185012.2:c.42G>A (NDUFA2)	NP_001171941.1:p.Leu14=
NR_033697.2:n.89G>A (NDUFA2)