Canonical Allele Identifier: CA1899313827
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313413T= , CM000672.2:g.30313413T= GRCh38
NC_000010.10:g.30602342T= , CM000672.1:g.30602342T= GRCh37
NC_000010.9:g.30642348T= NCBI36
NG_028096.1:g.40926A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*196A= MANE Select ENSP00000263063.3:n.*196A=
ENST00000263063.8:c.*196A= ENSP00000263063.3:n.*196A=
ENST00000488290.5:n.3700A=
NM_018109.3:c.*196A= NP_060579.3:n.*196A=
NM_018109.4:c.*196A= MANE Select NP_060579.3:n.*196A=