Canonical Allele Identifier: CA1899313838
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313438_30313439delinsAC , CM000672.2:g.30313438_30313439delinsAC GRCh38
NC_000010.10:g.30602367_30602368delinsAC , CM000672.1:g.30602367_30602368delinsAC GRCh37
NC_000010.9:g.30642373_30642374delinsAC NCBI36
NG_028096.1:g.40900_40901delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*170_*171delinsGT MANE Select ENSP00000263063.3:n.*170_*171delinsGT
ENST00000263063.8:c.*170_*171delinsGT ENSP00000263063.3:n.*170_*171delinsGT
ENST00000488290.5:n.3674_3675delinsGT
NM_018109.3:c.*170_*171delinsGT NP_060579.3:n.*170_*171delinsGT
NM_018109.4:c.*170_*171delinsGT MANE Select NP_060579.3:n.*170_*171delinsGT