Canonical Allele Identifier: CA1899313973

Gene: MTPAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30313732G= , CM000672.2:g.30313732G=	GRCh38
NC_000010.10:g.30602661G= , CM000672.1:g.30602661G=	GRCh37
NC_000010.9:g.30642667G=	NCBI36
NG_028096.1:g.40607C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263063.9:c.1626C= MANE Select	ENSP00000263063.3:p.Thr542=
ENST00000263063.8:c.1626C=	ENSP00000263063.3:p.Thr542=
ENST00000488290.5:n.3381C=
NM_018109.3:c.1626C=	NP_060579.3:p.Thr542=
NM_018109.4:c.1626C= MANE Select	NP_060579.3:p.Thr542=