Canonical Allele Identifier: CA1899313976
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313741C= , CM000672.2:g.30313741C= GRCh38
NC_000010.10:g.30602670C= , CM000672.1:g.30602670C= GRCh37
NC_000010.9:g.30642676C= NCBI36
NG_028096.1:g.40598G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263063.9:c.1617G= MANE Select ENSP00000263063.3:p.Lys539=
ENST00000263063.8:c.1617G= ENSP00000263063.3:p.Lys539=
ENST00000488290.5:n.3372G=
NM_018109.3:c.1617G= NP_060579.3:p.Lys539=
NM_018109.4:c.1617G= MANE Select NP_060579.3:p.Lys539=