Canonical Allele Identifier: CA663651055
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs1335302224
MyVariant Identifiers: chr10:g.30603161T>C (hg19) chr10:g.30314232T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314232T>C , CM000672.2:g.30314232T>C GRCh38
NC_000010.10:g.30603161T>C , CM000672.1:g.30603161T>C GRCh37
NC_000010.9:g.30643167T>C NCBI36
NG_028096.1:g.40107A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-261A>G MANE Select ENSP00000263063.3:n.1387-261A>G
ENST00000263063.8:c.1387-261A>G ENSP00000263063.3:n.1387-261A>G
ENST00000488290.5:n.3142-261A>G
NM_018109.3:c.1387-261A>G NP_060579.3:n.1387-261A>G
NM_018109.4:c.1387-261A>G MANE Select NP_060579.3:n.1387-261A>G
Search 100 bp 5'
Search 100 bp 3'