Canonical Allele Identifier: CA2787135313
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314145_30314146insACG , CM000672.2:g.30314145_30314146insACG GRCh38
NC_000010.10:g.30603074_30603075insACG , CM000672.1:g.30603074_30603075insACG GRCh37
NC_000010.9:g.30643080_30643081insACG NCBI36
NG_028096.1:g.40193_40194insCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-175_1387-174insCGT MANE Select ENSP00000263063.3:n.1387-175_1387-174insCGT
ENST00000263063.8:c.1387-175_1387-174insCGT ENSP00000263063.3:n.1387-175_1387-174insCGT
ENST00000488290.5:n.3142-175_3142-174insCGT
NM_018109.3:c.1387-175_1387-174insCGT NP_060579.3:n.1387-175_1387-174insCGT
NM_018109.4:c.1387-175_1387-174insCGT MANE Select NP_060579.3:n.1387-175_1387-174insCGT