Canonical Allele Identifier: CA1899313837
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313434T= , CM000672.2:g.30313434T= GRCh38
NC_000010.10:g.30602363T= , CM000672.1:g.30602363T= GRCh37
NC_000010.9:g.30642369T= NCBI36
NG_028096.1:g.40905A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*175A= MANE Select ENSP00000263063.3:n.*175A=
ENST00000263063.8:c.*175A= ENSP00000263063.3:n.*175A=
ENST00000488290.5:n.3679A=
NM_018109.3:c.*175A= NP_060579.3:n.*175A=
NM_018109.4:c.*175A= MANE Select NP_060579.3:n.*175A=