Canonical Allele Identifier: CA376433880
Gene: MTPAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313657T>A , CM000672.2:g.30313657T>A GRCh38
NC_000010.10:g.30602586T>A , CM000672.1:g.30602586T>A GRCh37
NC_000010.9:g.30642592T>A NCBI36
NG_028096.1:g.40682A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1701A>T MANE Select ENSP00000263063.3:p.Glu567Asp
ENST00000263063.8:c.1701A>T ENSP00000263063.3:p.Glu567Asp
ENST00000488290.5:n.3456A>T
NM_018109.3:c.1701A>T NP_060579.3:p.Glu567Asp
NM_018109.4:c.1701A>T MANE Select NP_060579.3:p.Glu567Asp