Canonical Allele Identifier: CA1899314091
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314015G= , CM000672.2:g.30314015G= GRCh38
NC_000010.10:g.30602944G= , CM000672.1:g.30602944G= GRCh37
NC_000010.9:g.30642950G= NCBI36
NG_028096.1:g.40324C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-44C= MANE Select ENSP00000263063.3:n.1387-44C=
ENST00000263063.8:c.1387-44C= ENSP00000263063.3:n.1387-44C=
ENST00000488290.5:n.3142-44C=
NM_018109.3:c.1387-44C= NP_060579.3:n.1387-44C=
NM_018109.4:c.1387-44C= MANE Select NP_060579.3:n.1387-44C=