Canonical Allele Identifier: CA1899314196

Gene: MTPAP

Linked Data

• dbSNP Id: rs1840635445

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30314266_30314274del , CM000672.2:g.30314266_30314274del	GRCh38
NC_000010.10:g.30603195_30603203del , CM000672.1:g.30603195_30603203del	GRCh37
NC_000010.9:g.30643201_30643209del	NCBI36
NG_028096.1:g.40067_40075del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263063.9:c.1387-301_1387-293del MANE Select	ENSP00000263063.3:n.1387-301_1387-293del
ENST00000263063.8:c.1387-301_1387-293del	ENSP00000263063.3:n.1387-301_1387-293del
ENST00000488290.5:n.3142-301_3142-293del
NM_018109.3:c.1387-301_1387-293del	NP_060579.3:n.1387-301_1387-293del
NM_018109.4:c.1387-301_1387-293del MANE Select	NP_060579.3:n.1387-301_1387-293del