Canonical Allele Identifier: CA1480088000

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622822G= , CM000666.2:g.99622822G=	GRCh38
NC_000004.11:g.100543979G= , CM000666.1:g.100543979G=	GRCh37
NC_000004.10:g.100763002G=	NCBI36
NG_011469.1:g.63740G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2659G= MANE Select	ENSP00000265517.5:p.Asp887=
ENST00000457717.6:c.2659G=	ENSP00000400821.1:p.Asp887=
ENST00000511045.6:c.2410G=	ENSP00000427679.2:p.Asp804=
ENST00000265517.9:c.2659G=	ENSP00000265517.5:p.Asp887=
ENST00000457717.5:c.2659G=	ENSP00000400821.1:p.Asp887=
ENST00000511045.5:c.2740G=	ENSP00000427679.1:p.Asp914=
ENST00000619629.1:c.*1106G=	ENSP00000482850.1:n.*1106G=
NM_000253.3:c.2659G=	NP_000244.2:p.Asp887=
NM_001300785.1:c.2740G=	NP_001287714.1:p.Asp914=
NM_000253.4:c.2659G=	NP_000244.2:p.Asp887=
NM_001300785.2:c.2410G=	NP_001287714.2:p.Asp804=
NM_001386140.1:c.2659G= MANE Select	NP_001373069.1:p.Asp887=