Canonical Allele Identifier: CA2224227395
Gene: MT2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609333C= , CM000678.2:g.56609333C= GRCh38
NC_000016.9:g.56643245C= , CM000678.1:g.56643245C= GRCh37
NC_000016.8:g.55200746C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.165C= MANE Select ENSP00000245185.5:p.Asp55=
ENST00000245185.5:c.165C= ENSP00000245185.5:p.Asp55=
ENST00000561491.1:c.*148C= ENSP00000456804.1:n.*148C=
ENST00000562017.1:n.739C=
ENST00000563985.1:n.545C=
ENST00000567300.1:n.252C=
NM_005953.3:c.165C= NP_005944.1:p.Asp55=
NM_005953.4:c.165C= NP_005944.1:p.Asp55=
NM_005953.5:c.165C= MANE Select NP_005944.1:p.Asp55=