Canonical Allele Identifier: CA1899313841
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313445A= , CM000672.2:g.30313445A= GRCh38
NC_000010.10:g.30602374A= , CM000672.1:g.30602374A= GRCh37
NC_000010.9:g.30642380A= NCBI36
NG_028096.1:g.40894T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*164T= MANE Select ENSP00000263063.3:n.*164T=
ENST00000263063.8:c.*164T= ENSP00000263063.3:n.*164T=
ENST00000488290.5:n.3668T=
NM_018109.3:c.*164T= NP_060579.3:n.*164T=
NM_018109.4:c.*164T= MANE Select NP_060579.3:n.*164T=