Canonical Allele Identifier: CA1899314131
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314126T= , CM000672.2:g.30314126T= GRCh38
NC_000010.10:g.30603055T= , CM000672.1:g.30603055T= GRCh37
NC_000010.9:g.30643061T= NCBI36
NG_028096.1:g.40213A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-155A= MANE Select ENSP00000263063.3:n.1387-155A=
ENST00000263063.8:c.1387-155A= ENSP00000263063.3:n.1387-155A=
ENST00000488290.5:n.3142-155A=
NM_018109.3:c.1387-155A= NP_060579.3:n.1387-155A=
NM_018109.4:c.1387-155A= MANE Select NP_060579.3:n.1387-155A=