Canonical Allele Identifier: CA1899313915
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313593C= , CM000672.2:g.30313593C= GRCh38
NC_000010.10:g.30602522C= , CM000672.1:g.30602522C= GRCh37
NC_000010.9:g.30642528C= NCBI36
NG_028096.1:g.40746G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*16G= MANE Select ENSP00000263063.3:n.*16G=
ENST00000263063.8:c.*16G= ENSP00000263063.3:n.*16G=
ENST00000488290.5:n.3520G=
NM_018109.3:c.*16G= NP_060579.3:n.*16G=
NM_018109.4:c.*16G= MANE Select NP_060579.3:n.*16G=