Canonical Allele Identifier: CA1899314139

Gene: MTPAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30314147_30314148delinsAT , CM000672.2:g.30314147_30314148delinsAT	GRCh38
NC_000010.10:g.30603076_30603077delinsAT , CM000672.1:g.30603076_30603077delinsAT	GRCh37
NC_000010.9:g.30643082_30643083delinsAT	NCBI36
NG_028096.1:g.40191_40192delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263063.9:c.1387-177_1387-176delinsAT MANE Select	ENSP00000263063.3:n.1387-177_1387-176delinsAT
ENST00000263063.8:c.1387-177_1387-176delinsAT	ENSP00000263063.3:n.1387-177_1387-176delinsAT
ENST00000488290.5:n.3142-177_3142-176delinsAT
NM_018109.3:c.1387-177_1387-176delinsAT	NP_060579.3:n.1387-177_1387-176delinsAT
NM_018109.4:c.1387-177_1387-176delinsAT MANE Select	NP_060579.3:n.1387-177_1387-176delinsAT