Canonical Allele Identifier: CA1899314188
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314245A= , CM000672.2:g.30314245A= GRCh38
NC_000010.10:g.30603174A= , CM000672.1:g.30603174A= GRCh37
NC_000010.9:g.30643180A= NCBI36
NG_028096.1:g.40094T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-274T= MANE Select ENSP00000263063.3:n.1387-274T=
ENST00000263063.8:c.1387-274T= ENSP00000263063.3:n.1387-274T=
ENST00000488290.5:n.3142-274T=
NM_018109.3:c.1387-274T= NP_060579.3:n.1387-274T=
NM_018109.4:c.1387-274T= MANE Select NP_060579.3:n.1387-274T=