Canonical Allele Identifier: CA1480088002

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622825A= , CM000666.2:g.99622825A=	GRCh38
NC_000004.11:g.100543982A= , CM000666.1:g.100543982A=	GRCh37
NC_000004.10:g.100763005A=	NCBI36
NG_011469.1:g.63743A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2662A= MANE Select	ENSP00000265517.5:p.Ser888=
ENST00000457717.6:c.2662A=	ENSP00000400821.1:p.Ser888=
ENST00000511045.6:c.2413A=	ENSP00000427679.2:p.Ser805=
ENST00000265517.9:c.2662A=	ENSP00000265517.5:p.Ser888=
ENST00000457717.5:c.2662A=	ENSP00000400821.1:p.Ser888=
ENST00000511045.5:c.2743A=	ENSP00000427679.1:p.Ser915=
ENST00000619629.1:c.*1109A=	ENSP00000482850.1:n.*1109A=
NM_000253.3:c.2662A=	NP_000244.2:p.Ser888=
NM_001300785.1:c.2743A=	NP_001287714.1:p.Ser915=
NM_000253.4:c.2662A=	NP_000244.2:p.Ser888=
NM_001300785.2:c.2413A=	NP_001287714.2:p.Ser805=
NM_001386140.1:c.2662A= MANE Select	NP_001373069.1:p.Ser888=