Canonical Allele Identifier: CA1899314224
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314329_30314330delinsGA , CM000672.2:g.30314329_30314330delinsGA GRCh38
NC_000010.10:g.30603258_30603259delinsGA , CM000672.1:g.30603258_30603259delinsGA GRCh37
NC_000010.9:g.30643264_30643265delinsGA NCBI36
NG_028096.1:g.40009_40010delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-359_1387-358delinsTC MANE Select ENSP00000263063.3:n.1387-359_1387-358delinsTC
ENST00000263063.8:c.1387-359_1387-358delinsTC ENSP00000263063.3:n.1387-359_1387-358delinsTC
ENST00000488290.5:n.3142-359_3142-358delinsTC
NM_018109.3:c.1387-359_1387-358delinsTC NP_060579.3:n.1387-359_1387-358delinsTC
NM_018109.4:c.1387-359_1387-358delinsTC MANE Select NP_060579.3:n.1387-359_1387-358delinsTC