Canonical Allele Identifier: CA1899314098
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314044_30314045delinsTA , CM000672.2:g.30314044_30314045delinsTA GRCh38
NC_000010.10:g.30602973_30602974delinsTA , CM000672.1:g.30602973_30602974delinsTA GRCh37
NC_000010.9:g.30642979_30642980delinsTA NCBI36
NG_028096.1:g.40294_40295delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-74_1387-73delinsTA MANE Select ENSP00000263063.3:n.1387-74_1387-73delinsTA
ENST00000263063.8:c.1387-74_1387-73delinsTA ENSP00000263063.3:n.1387-74_1387-73delinsTA
ENST00000488290.5:n.3142-74_3142-73delinsTA
NM_018109.3:c.1387-74_1387-73delinsTA NP_060579.3:n.1387-74_1387-73delinsTA
NM_018109.4:c.1387-74_1387-73delinsTA MANE Select NP_060579.3:n.1387-74_1387-73delinsTA