Canonical Allele Identifier: CA1899314208
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314279_30314284delinsGTATTT , CM000672.2:g.30314279_30314284delinsGTATTT GRCh38
NC_000010.10:g.30603208_30603213delinsGTATTT , CM000672.1:g.30603208_30603213delinsGTATTT GRCh37
NC_000010.9:g.30643214_30643219delinsGTATTT NCBI36
NG_028096.1:g.40055_40060delinsAAATAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-313_1387-308delinsAAATAC MANE Select ENSP00000263063.3:n.1387-313_1387-308delinsAAATAC
ENST00000263063.8:c.1387-313_1387-308delinsAAATAC ENSP00000263063.3:n.1387-313_1387-308delinsAAATAC
ENST00000488290.5:n.3142-313_3142-308delinsAAATAC
NM_018109.3:c.1387-313_1387-308delinsAAATAC NP_060579.3:n.1387-313_1387-308delinsAAATAC
NM_018109.4:c.1387-313_1387-308delinsAAATAC MANE Select NP_060579.3:n.1387-313_1387-308delinsAAATAC