Canonical Allele Identifier: CA1899313904
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313576C= , CM000672.2:g.30313576C= GRCh38
NC_000010.10:g.30602505C= , CM000672.1:g.30602505C= GRCh37
NC_000010.9:g.30642511C= NCBI36
NG_028096.1:g.40763G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*33G= MANE Select ENSP00000263063.3:n.*33G=
ENST00000263063.8:c.*33G= ENSP00000263063.3:n.*33G=
ENST00000488290.5:n.3537G=
NM_018109.3:c.*33G= NP_060579.3:n.*33G=
NM_018109.4:c.*33G= MANE Select NP_060579.3:n.*33G=