Canonical Allele Identifier: CA2608695568
Gene: MTPAP HGNC NCBI

Linked Data

gnomAD v4: 10-30313402-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313402T>G , CM000672.2:g.30313402T>G GRCh38
NC_000010.10:g.30602331T>G , CM000672.1:g.30602331T>G GRCh37
NC_000010.9:g.30642337T>G NCBI36
NG_028096.1:g.40937A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*207A>C MANE Select ENSP00000263063.3:n.*207A>C
ENST00000263063.8:c.*207A>C ENSP00000263063.3:n.*207A>C
ENST00000488290.5:n.3711A>C
NM_018109.3:c.*207A>C NP_060579.3:n.*207A>C
NM_018109.4:c.*207A>C MANE Select NP_060579.3:n.*207A>C
Search 100 bp 5'
Search 100 bp 3'