Canonical Allele Identifier: CA352727363
Gene: NDUFAF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49022394T>G , CM000665.2:g.49022394T>G GRCh38
NC_000003.11:g.49059827T>G , CM000665.1:g.49059827T>G GRCh37
NC_000003.10:g.49034831T>G NCBI36
NG_012091.1:g.12049A>C
NG_016282.1:g.6920T>G
NG_033126.1:g.3678A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326925.11:c.126T>G MANE Select ENSP00000323076.5:p.Tyr42Ter
ENST00000326912.8:c.-46T>G ENSP00000323003.4:n.-46T>G
ENST00000326925.10:c.126T>G ENSP00000323076.5:p.Tyr42Ter
ENST00000395458.6:c.-46T>G ENSP00000378843.2:n.-46T>G
ENST00000451378.2:c.-46T>G ENSP00000402465.2:n.-46T>G
ENST00000480392.1:n.150T>G
ENST00000496152.1:n.282T>G
NM_199069.1:c.126T>G NP_951032.1:p.Tyr42Ter
NM_199070.1:c.-46T>G NP_951033.1:n.-46T>G
NM_199073.1:c.-46T>G NP_951047.1:n.-46T>G
NM_199074.1:c.-46T>G NP_951056.1:n.-46T>G
NM_199069.2:c.126T>G MANE Select NP_951032.1:p.Tyr42Ter
NM_199070.2:c.-46T>G NP_951033.1:n.-46T>G
NM_199073.2:c.-46T>G NP_951047.1:n.-46T>G
NM_199074.2:c.-46T>G NP_951056.1:n.-46T>G