Canonical Allele Identifier: CA1480066693

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583416G= , CM000666.2:g.99583416G=	GRCh38
NC_000004.11:g.100504573G= , CM000666.1:g.100504573G=	GRCh37
NC_000004.10:g.100723596G=	NCBI36
NG_011469.1:g.24334G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.292G= MANE Select	ENSP00000265517.5:p.Glu98=
ENST00000457717.6:c.292G=	ENSP00000400821.1:p.Glu98=
ENST00000505094.6:c.43G=	ENSP00000422782.2:p.Glu15=
ENST00000511045.6:c.43G=	ENSP00000427679.2:p.Glu15=
ENST00000265517.9:c.292G=	ENSP00000265517.5:p.Glu98=
ENST00000422897.6:c.292G=	ENSP00000407350.2:p.Glu98=
ENST00000457717.5:c.292G=	ENSP00000400821.1:p.Glu98=
ENST00000505094.5:c.*382G=	ENSP00000422782.1:n.*382G=
ENST00000506883.5:c.322G=	ENSP00000426755.1:p.Glu108=
ENST00000511045.5:c.373G=	ENSP00000427679.1:p.Glu125=
ENST00000513404.5:c.*355G=	ENSP00000424972.1:n.*355G=
ENST00000515141.5:c.*355G=	ENSP00000425642.1:n.*355G=
ENST00000619629.1:c.292G=	ENSP00000482850.1:p.Glu98=
NM_000253.3:c.292G=	NP_000244.2:p.Glu98=
NM_001300785.1:c.373G=	NP_001287714.1:p.Glu125=
NM_000253.4:c.292G=	NP_000244.2:p.Glu98=
NM_001300785.2:c.43G=	NP_001287714.2:p.Glu15=
NM_001386140.1:c.292G= MANE Select	NP_001373069.1:p.Glu98=