Canonical Allele Identifier: CA1899313848
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313455_30313456delinsAC , CM000672.2:g.30313455_30313456delinsAC GRCh38
NC_000010.10:g.30602384_30602385delinsAC , CM000672.1:g.30602384_30602385delinsAC GRCh37
NC_000010.9:g.30642390_30642391delinsAC NCBI36
NG_028096.1:g.40883_40884delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*153_*154delinsGT MANE Select ENSP00000263063.3:n.*153_*154delinsGT
ENST00000263063.8:c.*153_*154delinsGT ENSP00000263063.3:n.*153_*154delinsGT
ENST00000488290.5:n.3657_3658delinsGT
NM_018109.3:c.*153_*154delinsGT NP_060579.3:n.*153_*154delinsGT
NM_018109.4:c.*153_*154delinsGT MANE Select NP_060579.3:n.*153_*154delinsGT