Canonical Allele Identifier: CA1899314195
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314263_30314272delinsAACTCAACCG , CM000672.2:g.30314263_30314272delinsAACTCAACCG GRCh38
NC_000010.10:g.30603192_30603201delinsAACTCAACCG , CM000672.1:g.30603192_30603201delinsAACTCAACCG GRCh37
NC_000010.9:g.30643198_30643207delinsAACTCAACCG NCBI36
NG_028096.1:g.40067_40076delinsCGGTTGAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-301_1387-292delinsCGGTTGAGTT MANE Select ENSP00000263063.3:n.1387-301_1387-292delinsCGGTTGAGTT
ENST00000263063.8:c.1387-301_1387-292delinsCGGTTGAGTT ENSP00000263063.3:n.1387-301_1387-292delinsCGGTTGAGTT
ENST00000488290.5:n.3142-301_3142-292delinsCGGTTGAGTT
NM_018109.3:c.1387-301_1387-292delinsCGGTTGAGTT NP_060579.3:n.1387-301_1387-292delinsCGGTTGAGTT
NM_018109.4:c.1387-301_1387-292delinsCGGTTGAGTT MANE Select NP_060579.3:n.1387-301_1387-292delinsCGGTTGAGTT