Canonical Allele Identifier: CA1899313903
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313575G= , CM000672.2:g.30313575G= GRCh38
NC_000010.10:g.30602504G= , CM000672.1:g.30602504G= GRCh37
NC_000010.9:g.30642510G= NCBI36
NG_028096.1:g.40764C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*34C= MANE Select ENSP00000263063.3:n.*34C=
ENST00000263063.8:c.*34C= ENSP00000263063.3:n.*34C=
ENST00000488290.5:n.3538C=
NM_018109.3:c.*34C= NP_060579.3:n.*34C=
NM_018109.4:c.*34C= MANE Select NP_060579.3:n.*34C=