Canonical Allele Identifier: CA1899314218
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs1840635824

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314315_30314318dup , CM000672.2:g.30314315_30314318dup GRCh38
NC_000010.10:g.30603244_30603247dup , CM000672.1:g.30603244_30603247dup GRCh37
NC_000010.9:g.30643250_30643253dup NCBI36
NG_028096.1:g.40021_40024dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-347_1387-344dup MANE Select ENSP00000263063.3:n.1387-347_1387-344dup
ENST00000263063.8:c.1387-347_1387-344dup ENSP00000263063.3:n.1387-347_1387-344dup
ENST00000488290.5:n.3142-347_3142-344dup
NM_018109.3:c.1387-347_1387-344dup NP_060579.3:n.1387-347_1387-344dup
NM_018109.4:c.1387-347_1387-344dup MANE Select NP_060579.3:n.1387-347_1387-344dup