Canonical Allele Identifier: CA1899313979

Gene: MTPAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30313751G= , CM000672.2:g.30313751G=	GRCh38
NC_000010.10:g.30602680G= , CM000672.1:g.30602680G=	GRCh37
NC_000010.9:g.30642686G=	NCBI36
NG_028096.1:g.40588C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263063.9:c.1607C= MANE Select	ENSP00000263063.3:p.Pro536=
ENST00000263063.8:c.1607C=	ENSP00000263063.3:p.Pro536=
ENST00000488290.5:n.3362C=
NM_018109.3:c.1607C=	NP_060579.3:p.Pro536=
NM_018109.4:c.1607C= MANE Select	NP_060579.3:p.Pro536=