Canonical Allele Identifier: CA653680821

Gene: MTPAP

Linked Data

• COSMIC: COSN16131000

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30313482_30313483insC , CM000672.2:g.30313482_30313483insC	GRCh38
NC_000010.10:g.30602411_30602412insC , CM000672.1:g.30602411_30602412insC	GRCh37
NC_000010.9:g.30642417_30642418insC	NCBI36
NG_028096.1:g.40856_40857insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263063.9:c.*126_*127insG MANE Select	ENSP00000263063.3:n.*126_*127insG
ENST00000263063.8:c.*126_*127insG	ENSP00000263063.3:n.*126_*127insG
ENST00000488290.5:n.3630_3631insG
NM_018109.3:c.*126_*127insG	NP_060579.3:n.*126_*127insG
NM_018109.4:c.*126_*127insG MANE Select	NP_060579.3:n.*126_*127insG