Canonical Allele Identifier: CA1899314228
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314353A= , CM000672.2:g.30314353A= GRCh38
NC_000010.10:g.30603282A= , CM000672.1:g.30603282A= GRCh37
NC_000010.9:g.30643288A= NCBI36
NG_028096.1:g.39986T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-382T= MANE Select ENSP00000263063.3:n.1387-382T=
ENST00000263063.8:c.1387-382T= ENSP00000263063.3:n.1387-382T=
ENST00000488290.5:n.3142-382T=
NM_018109.3:c.1387-382T= NP_060579.3:n.1387-382T=
NM_018109.4:c.1387-382T= MANE Select NP_060579.3:n.1387-382T=