Canonical Allele Identifier: CA1899313833
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313423T= , CM000672.2:g.30313423T= GRCh38
NC_000010.10:g.30602352T= , CM000672.1:g.30602352T= GRCh37
NC_000010.9:g.30642358T= NCBI36
NG_028096.1:g.40916A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*186A= MANE Select ENSP00000263063.3:n.*186A=
ENST00000263063.8:c.*186A= ENSP00000263063.3:n.*186A=
ENST00000488290.5:n.3690A=
NM_018109.3:c.*186A= NP_060579.3:n.*186A=
NM_018109.4:c.*186A= MANE Select NP_060579.3:n.*186A=