Canonical Allele Identifier: CA1899314200
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs1840635489
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314270C>T , CM000672.2:g.30314270C>T GRCh38
NC_000010.10:g.30603199C>T , CM000672.1:g.30603199C>T GRCh37
NC_000010.9:g.30643205C>T NCBI36
NG_028096.1:g.40069G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-299G>A MANE Select ENSP00000263063.3:n.1387-299G>A
ENST00000263063.8:c.1387-299G>A ENSP00000263063.3:n.1387-299G>A
ENST00000488290.5:n.3142-299G>A
NM_018109.3:c.1387-299G>A NP_060579.3:n.1387-299G>A
NM_018109.4:c.1387-299G>A MANE Select NP_060579.3:n.1387-299G>A
Search 100 bp 5'
Search 100 bp 3'