Canonical Allele Identifier: CA1899313971

Gene: MTPAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30313726C= , CM000672.2:g.30313726C=	GRCh38
NC_000010.10:g.30602655C= , CM000672.1:g.30602655C=	GRCh37
NC_000010.9:g.30642661C=	NCBI36
NG_028096.1:g.40613G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263063.9:c.1632G= MANE Select	ENSP00000263063.3:p.Lys544=
ENST00000263063.8:c.1632G=	ENSP00000263063.3:p.Lys544=
ENST00000488290.5:n.3387G=
NM_018109.3:c.1632G=	NP_060579.3:p.Lys544=
NM_018109.4:c.1632G= MANE Select	NP_060579.3:p.Lys544=