Canonical Allele Identifier: CA1899313969
Gene: MTPAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313721C= , CM000672.2:g.30313721C= GRCh38
NC_000010.10:g.30602650C= , CM000672.1:g.30602650C= GRCh37
NC_000010.9:g.30642656C= NCBI36
NG_028096.1:g.40618G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1637G= MANE Select ENSP00000263063.3:p.Ser546=
ENST00000263063.8:c.1637G= ENSP00000263063.3:p.Ser546=
ENST00000488290.5:n.3392G=
NM_018109.3:c.1637G= NP_060579.3:p.Ser546=
NM_018109.4:c.1637G= MANE Select NP_060579.3:p.Ser546=
Search 100 bp 5'
Search 100 bp 3'