Canonical Allele Identifier: CA1899314176
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314223_30314226delinsGGAT , CM000672.2:g.30314223_30314226delinsGGAT GRCh38
NC_000010.10:g.30603152_30603155delinsGGAT , CM000672.1:g.30603152_30603155delinsGGAT GRCh37
NC_000010.9:g.30643158_30643161delinsGGAT NCBI36
NG_028096.1:g.40113_40116delinsATCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-255_1387-252delinsATCC MANE Select ENSP00000263063.3:n.1387-255_1387-252delinsATCC
ENST00000263063.8:c.1387-255_1387-252delinsATCC ENSP00000263063.3:n.1387-255_1387-252delinsATCC
ENST00000488290.5:n.3142-255_3142-252delinsATCC
NM_018109.3:c.1387-255_1387-252delinsATCC NP_060579.3:n.1387-255_1387-252delinsATCC
NM_018109.4:c.1387-255_1387-252delinsATCC MANE Select NP_060579.3:n.1387-255_1387-252delinsATCC