Canonical Allele Identifier: CA2787135292

Gene: MTPAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30314102_30314103insAC , CM000672.2:g.30314102_30314103insAC	GRCh38
NC_000010.10:g.30603031_30603032insAC , CM000672.1:g.30603031_30603032insAC	GRCh37
NC_000010.9:g.30643037_30643038insAC	NCBI36
NG_028096.1:g.40237_40238insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263063.9:c.1387-131_1387-130insTG MANE Select	ENSP00000263063.3:n.1387-131_1387-130insTG
ENST00000263063.8:c.1387-131_1387-130insTG	ENSP00000263063.3:n.1387-131_1387-130insTG
ENST00000488290.5:n.3142-131_3142-130insTG
NM_018109.3:c.1387-131_1387-130insTG	NP_060579.3:n.1387-131_1387-130insTG
NM_018109.4:c.1387-131_1387-130insTG MANE Select	NP_060579.3:n.1387-131_1387-130insTG