Canonical Allele Identifier: CA1899313939
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313650T= , CM000672.2:g.30313650T= GRCh38
NC_000010.10:g.30602579T= , CM000672.1:g.30602579T= GRCh37
NC_000010.9:g.30642585T= NCBI36
NG_028096.1:g.40689A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1708A= MANE Select ENSP00000263063.3:p.Thr570=
ENST00000263063.8:c.1708A= ENSP00000263063.3:p.Thr570=
ENST00000488290.5:n.3463A=
NM_018109.3:c.1708A= NP_060579.3:p.Thr570=
NM_018109.4:c.1708A= MANE Select NP_060579.3:p.Thr570=