Canonical Allele Identifier: CA1899314147
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs906987231

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314163_30314164dup , CM000672.2:g.30314163_30314164dup GRCh38
NC_000010.10:g.30603092_30603093dup , CM000672.1:g.30603092_30603093dup GRCh37
NC_000010.9:g.30643098_30643099dup NCBI36
NG_028096.1:g.40183_40184dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-185_1387-184dup MANE Select ENSP00000263063.3:n.1387-185_1387-184dup
ENST00000263063.8:c.1387-185_1387-184dup ENSP00000263063.3:n.1387-185_1387-184dup
ENST00000488290.5:n.3142-185_3142-184dup
NM_018109.3:c.1387-185_1387-184dup NP_060579.3:n.1387-185_1387-184dup
NM_018109.4:c.1387-185_1387-184dup MANE Select NP_060579.3:n.1387-185_1387-184dup