Canonical Allele Identifier: CA1899313840
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313441G= , CM000672.2:g.30313441G= GRCh38
NC_000010.10:g.30602370G= , CM000672.1:g.30602370G= GRCh37
NC_000010.9:g.30642376G= NCBI36
NG_028096.1:g.40898C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*168C= MANE Select ENSP00000263063.3:n.*168C=
ENST00000263063.8:c.*168C= ENSP00000263063.3:n.*168C=
ENST00000488290.5:n.3672C=
NM_018109.3:c.*168C= NP_060579.3:n.*168C=
NM_018109.4:c.*168C= MANE Select NP_060579.3:n.*168C=