Canonical Allele Identifier: CA1899313922
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313611A= , CM000672.2:g.30313611A= GRCh38
NC_000010.10:g.30602540A= , CM000672.1:g.30602540A= GRCh37
NC_000010.9:g.30642546A= NCBI36
NG_028096.1:g.40728T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1747T= MANE Select ENSP00000263063.3:p.Ter583=
ENST00000263063.8:c.1747T= ENSP00000263063.3:p.Ter583=
ENST00000488290.5:n.3502T=
NM_018109.3:c.1747T= NP_060579.3:p.Ter583=
NM_018109.4:c.1747T= MANE Select NP_060579.3:p.Ter583=