Canonical Allele Identifier: CA1899313844
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313448T= , CM000672.2:g.30313448T= GRCh38
NC_000010.10:g.30602377T= , CM000672.1:g.30602377T= GRCh37
NC_000010.9:g.30642383T= NCBI36
NG_028096.1:g.40891A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*161A= MANE Select ENSP00000263063.3:n.*161A=
ENST00000263063.8:c.*161A= ENSP00000263063.3:n.*161A=
ENST00000488290.5:n.3665A=
NM_018109.3:c.*161A= NP_060579.3:n.*161A=
NM_018109.4:c.*161A= MANE Select NP_060579.3:n.*161A=