Canonical Allele Identifier: CA205300650
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs35331130

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313391dup , CM000672.2:g.30313391dup GRCh38
NC_000010.10:g.30602320dup , CM000672.1:g.30602320dup GRCh37
NC_000010.9:g.30642326dup NCBI36
NG_028096.1:g.40949dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*219dup MANE Select ENSP00000263063.3:n.*219dup
ENST00000263063.8:c.*219dup ENSP00000263063.3:n.*219dup
ENST00000488290.5:n.3723dup
NM_018109.3:c.*219dup NP_060579.3:n.*219dup
NM_018109.4:c.*219dup MANE Select NP_060579.3:n.*219dup