Canonical Allele Identifier: CA1899314143
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314154_30314155delinsGT , CM000672.2:g.30314154_30314155delinsGT GRCh38
NC_000010.10:g.30603083_30603084delinsGT , CM000672.1:g.30603083_30603084delinsGT GRCh37
NC_000010.9:g.30643089_30643090delinsGT NCBI36
NG_028096.1:g.40184_40185delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-184_1387-183delinsAC MANE Select ENSP00000263063.3:n.1387-184_1387-183delinsAC
ENST00000263063.8:c.1387-184_1387-183delinsAC ENSP00000263063.3:n.1387-184_1387-183delinsAC
ENST00000488290.5:n.3142-184_3142-183delinsAC
NM_018109.3:c.1387-184_1387-183delinsAC NP_060579.3:n.1387-184_1387-183delinsAC
NM_018109.4:c.1387-184_1387-183delinsAC MANE Select NP_060579.3:n.1387-184_1387-183delinsAC