Canonical Allele Identifier: CA3442585

Gene: NDUFA2 IK

Linked Data

• dbSNP Id: rs369495222
• ExAC: 5:140027211 A / C
• gnomAD v2: 5-140027211-A-C
• gnomAD v3: 5-140647626-A-C
• gnomAD v4: 5-140647626-A-C
• MyVariant Identifiers: chr5:g.140027211A>C (hg19) ; chr5:g.140647626A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140647626A>C , CM000667.2:g.140647626A>C	GRCh38
NC_000005.9:g.140027211A>C , CM000667.1:g.140027211A>C	GRCh37
NC_000005.8:g.140007395A>C	NCBI36
NG_021417.1:g.5160T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252102.9:c.-43T>G (NDUFA2) MANE Select	ENSP00000252102.5:n.-43T>G
ENST00000252102.8:c.-43T>G (NDUFA2)	ENSP00000252102.4:n.-43T>G
ENST00000502960.1:n.146T>G (NDUFA2)
ENST00000512088.1:c.-43T>G (NDUFA2)	ENSP00000427220.1:n.-43T>G
ENST00000513256.5:c.4+317A>C (IK)	ENSP00000425564.1:n.4+317A>C
NM_001185012.1:c.-43T>G (NDUFA2)	NP_001171941.1:n.-43T>G
NM_002488.4:c.-43T>G (NDUFA2)	NP_002479.1:n.-43T>G
NR_033697.1:n.160T>G (NDUFA2)
NM_002488.5:c.-43T>G (NDUFA2) MANE Select	NP_002479.1:n.-43T>G
NM_001185012.2:c.-43T>G (NDUFA2)	NP_001171941.1:n.-43T>G
NR_033697.2:n.5T>G (NDUFA2)