Canonical Allele Identifier: CA1899314044
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313929G= , CM000672.2:g.30313929G= GRCh38
NC_000010.10:g.30602858G= , CM000672.1:g.30602858G= GRCh37
NC_000010.9:g.30642864G= NCBI36
NG_028096.1:g.40410C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263063.9:c.1429C= MANE Select ENSP00000263063.3:p.Gln477=
ENST00000263063.8:c.1429C= ENSP00000263063.3:p.Gln477=
ENST00000488290.5:n.3184C=
NM_018109.3:c.1429C= NP_060579.3:p.Gln477=
NM_018109.4:c.1429C= MANE Select NP_060579.3:p.Gln477=