Canonical Allele Identifier: CA645544917
Gene: MTPAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313871del , CM000672.2:g.30313871del GRCh38
NC_000010.10:g.30602800del , CM000672.1:g.30602800del GRCh37
NC_000010.9:g.30642806del NCBI36
NG_028096.1:g.40472del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1491del MANE Select ENSP00000263063.3:p.Lys497AsnfsTer3
ENST00000263063.8:c.1491del ENSP00000263063.3:p.Lys497AsnfsTer3
ENST00000488290.5:n.3246del
NM_018109.3:c.1491del NP_060579.3:p.Lys497AsnfsTer3
NM_018109.4:c.1491del MANE Select NP_060579.3:p.Lys497AsnfsTer3