Canonical Allele Identifier: CA1899313813
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313390C= , CM000672.2:g.30313390C= GRCh38
NC_000010.10:g.30602319C= , CM000672.1:g.30602319C= GRCh37
NC_000010.9:g.30642325C= NCBI36
NG_028096.1:g.40949G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*219G= MANE Select ENSP00000263063.3:n.*219G=
ENST00000263063.8:c.*219G= ENSP00000263063.3:n.*219G=
ENST00000488290.5:n.3723G=
NM_018109.3:c.*219G= NP_060579.3:n.*219G=
NM_018109.4:c.*219G= MANE Select NP_060579.3:n.*219G=