Canonical Allele Identifier: CA1899313856
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313471_30313472delinsAG , CM000672.2:g.30313471_30313472delinsAG GRCh38
NC_000010.10:g.30602400_30602401delinsAG , CM000672.1:g.30602400_30602401delinsAG GRCh37
NC_000010.9:g.30642406_30642407delinsAG NCBI36
NG_028096.1:g.40867_40868delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*137_*138delinsCT MANE Select ENSP00000263063.3:n.*137_*138delinsCT
ENST00000263063.8:c.*137_*138delinsCT ENSP00000263063.3:n.*137_*138delinsCT
ENST00000488290.5:n.3641_3642delinsCT
NM_018109.3:c.*137_*138delinsCT NP_060579.3:n.*137_*138delinsCT
NM_018109.4:c.*137_*138delinsCT MANE Select NP_060579.3:n.*137_*138delinsCT