Canonical Allele Identifier: CA1480058926

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99574331G= , CM000666.2:g.99574331G=	GRCh38
NC_000004.11:g.100495488G= , CM000666.1:g.100495488G=	GRCh37
NC_000004.10:g.100714511G=	NCBI36
NG_011469.1:g.15249G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457717.6:c.-101-478G=	ENSP00000400821.1:n.-101-478G=
ENST00000505094.6:c.-189+3466G=	ENSP00000422782.2:n.-189+3466G=
ENST00000511045.6:c.-188-7574G=	ENSP00000427679.2:n.-188-7574G=
ENST00000511610.6:c.-101-478G=	ENSP00000422178.2:n.-101-478G=
ENST00000457717.5:c.-101-478G=	ENSP00000400821.1:n.-101-478G=
ENST00000504724.1:c.*327-478G=	ENSP00000422667.1:n.*327-478G=
ENST00000505094.5:c.*151+3466G=	ENSP00000422782.1:n.*151+3466G=
ENST00000505142.5:c.*90-478G=	ENSP00000425987.1:n.*90-478G=
ENST00000506883.5:c.92-7574G=	ENSP00000426755.1:n.92-7574G=
ENST00000511045.5:c.143-7574G=	ENSP00000427679.1:n.143-7574G=
ENST00000511610.5:c.*90-478G=	ENSP00000422178.1:n.*90-478G=
ENST00000513404.5:c.92-478G=	ENSP00000424972.1:n.92-478G=
ENST00000515141.5:c.143-478G=	ENSP00000425642.1:n.143-478G=
NM_000253.3:c.-101-478G=	NP_000244.2:n.-101-478G=
NM_001300785.1:c.143-7574G=	NP_001287714.1:n.143-7574G=
NM_000253.4:c.-101-478G=	NP_000244.2:n.-101-478G=
NM_001300785.2:c.-188-7574G=	NP_001287714.2:n.-188-7574G=