Canonical Allele Identifier: CA1899314141
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314151_30314154delinsTTTG , CM000672.2:g.30314151_30314154delinsTTTG GRCh38
NC_000010.10:g.30603080_30603083delinsTTTG , CM000672.1:g.30603080_30603083delinsTTTG GRCh37
NC_000010.9:g.30643086_30643089delinsTTTG NCBI36
NG_028096.1:g.40185_40188delinsCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-183_1387-180delinsCAAA MANE Select ENSP00000263063.3:n.1387-183_1387-180delinsCAAA
ENST00000263063.8:c.1387-183_1387-180delinsCAAA ENSP00000263063.3:n.1387-183_1387-180delinsCAAA
ENST00000488290.5:n.3142-183_3142-180delinsCAAA
NM_018109.3:c.1387-183_1387-180delinsCAAA NP_060579.3:n.1387-183_1387-180delinsCAAA
NM_018109.4:c.1387-183_1387-180delinsCAAA MANE Select NP_060579.3:n.1387-183_1387-180delinsCAAA