Canonical Allele Identifier: CA1899313861
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313475G= , CM000672.2:g.30313475G= GRCh38
NC_000010.10:g.30602404G= , CM000672.1:g.30602404G= GRCh37
NC_000010.9:g.30642410G= NCBI36
NG_028096.1:g.40864C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*134C= MANE Select ENSP00000263063.3:n.*134C=
ENST00000263063.8:c.*134C= ENSP00000263063.3:n.*134C=
ENST00000488290.5:n.3638C=
NM_018109.3:c.*134C= NP_060579.3:n.*134C=
NM_018109.4:c.*134C= MANE Select NP_060579.3:n.*134C=