Canonical Allele Identifier: CA1899314230
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314361_30314364delinsTGAA , CM000672.2:g.30314361_30314364delinsTGAA GRCh38
NC_000010.10:g.30603290_30603293delinsTGAA , CM000672.1:g.30603290_30603293delinsTGAA GRCh37
NC_000010.9:g.30643296_30643299delinsTGAA NCBI36
NG_028096.1:g.39975_39978delinsTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-393_1387-390delinsTTCA MANE Select ENSP00000263063.3:n.1387-393_1387-390delinsTTCA
ENST00000263063.8:c.1387-393_1387-390delinsTTCA ENSP00000263063.3:n.1387-393_1387-390delinsTTCA
ENST00000488290.5:n.3142-393_3142-390delinsTTCA
NM_018109.3:c.1387-393_1387-390delinsTTCA NP_060579.3:n.1387-393_1387-390delinsTTCA
NM_018109.4:c.1387-393_1387-390delinsTTCA MANE Select NP_060579.3:n.1387-393_1387-390delinsTTCA