Canonical Allele Identifier: CA2787135254
Gene: MTPAP HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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