Canonical Allele Identifier: CA1899313836
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313430C= , CM000672.2:g.30313430C= GRCh38
NC_000010.10:g.30602359C= , CM000672.1:g.30602359C= GRCh37
NC_000010.9:g.30642365C= NCBI36
NG_028096.1:g.40909G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*179G= MANE Select ENSP00000263063.3:n.*179G=
ENST00000263063.8:c.*179G= ENSP00000263063.3:n.*179G=
ENST00000488290.5:n.3683G=
NM_018109.3:c.*179G= NP_060579.3:n.*179G=
NM_018109.4:c.*179G= MANE Select NP_060579.3:n.*179G=