Canonical Allele Identifier: CA1899313824
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313406A= , CM000672.2:g.30313406A= GRCh38
NC_000010.10:g.30602335A= , CM000672.1:g.30602335A= GRCh37
NC_000010.9:g.30642341A= NCBI36
NG_028096.1:g.40933T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*203T= MANE Select ENSP00000263063.3:n.*203T=
ENST00000263063.8:c.*203T= ENSP00000263063.3:n.*203T=
ENST00000488290.5:n.3707T=
NM_018109.3:c.*203T= NP_060579.3:n.*203T=
NM_018109.4:c.*203T= MANE Select NP_060579.3:n.*203T=