Canonical Allele Identifier: CA1969458340
Community Standard Title: NM_004551.3(NDUFS3):c.2T= (p.Met1=)
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47579093T= , CM000673.2:g.47579093T= GRCh38
NC_000011.9:g.47600645T= , CM000673.1:g.47600645T= GRCh37
NC_000011.8:g.47557221T= NCBI36
NG_011946.1:g.5084T=
NG_011946.2:g.5084T=

Transcript Alleles

HGVS Amino-acid Change
NM_004551.3:c.2T= MANE Select NP_004542.1:p.Met1=
ENST00000263774.9:c.2T= MANE Select ENSP00000263774.4:p.Met1=
NM_004551.2:c.2T= NP_004542.1:p.Met1=
ENST00000263774.8:c.2T= ENSP00000263774.4:p.Met1=
ENST00000528192.5:c.2T= ENSP00000432099.1:p.Met1=
ENST00000529276.1:c.2T= ENSP00000433753.1:p.Met1=
ENST00000530295.5:c.2T= ENSP00000431588.1:p.Met1=
ENST00000533105.1:n.9T=
ENST00000533507.5:n.816-1432T=
ENST00000534208.5:c.2T= ENSP00000433405.1:p.Met1=
ENST00000534716.2:c.2T= ENSP00000434970.2:p.Met1=