Canonical Allele Identifier: CA1899313839
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313439C= , CM000672.2:g.30313439C= GRCh38
NC_000010.10:g.30602368C= , CM000672.1:g.30602368C= GRCh37
NC_000010.9:g.30642374C= NCBI36
NG_028096.1:g.40900G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*170G= MANE Select ENSP00000263063.3:n.*170G=
ENST00000263063.8:c.*170G= ENSP00000263063.3:n.*170G=
ENST00000488290.5:n.3674G=
NM_018109.3:c.*170G= NP_060579.3:n.*170G=
NM_018109.4:c.*170G= MANE Select NP_060579.3:n.*170G=