Canonical Allele Identifier: CA1899313857
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs1840622528

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313476del , CM000672.2:g.30313476del GRCh38
NC_000010.10:g.30602405del , CM000672.1:g.30602405del GRCh37
NC_000010.9:g.30642411del NCBI36
NG_028096.1:g.40867del

Transcript Alleles

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