Canonical Allele Identifier: CA1899314115
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314084A= , CM000672.2:g.30314084A= GRCh38
NC_000010.10:g.30603013A= , CM000672.1:g.30603013A= GRCh37
NC_000010.9:g.30643019A= NCBI36
NG_028096.1:g.40255T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-113T= MANE Select ENSP00000263063.3:n.1387-113T=
ENST00000263063.8:c.1387-113T= ENSP00000263063.3:n.1387-113T=
ENST00000488290.5:n.3142-113T=
NM_018109.3:c.1387-113T= NP_060579.3:n.1387-113T=
NM_018109.4:c.1387-113T= MANE Select NP_060579.3:n.1387-113T=