Canonical Allele Identifier: CA1899314138
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314138G= , CM000672.2:g.30314138G= GRCh38
NC_000010.10:g.30603067G= , CM000672.1:g.30603067G= GRCh37
NC_000010.9:g.30643073G= NCBI36
NG_028096.1:g.40201C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-167C= MANE Select ENSP00000263063.3:n.1387-167C=
ENST00000263063.8:c.1387-167C= ENSP00000263063.3:n.1387-167C=
ENST00000488290.5:n.3142-167C=
NM_018109.3:c.1387-167C= NP_060579.3:n.1387-167C=
NM_018109.4:c.1387-167C= MANE Select NP_060579.3:n.1387-167C=