Canonical Allele Identifier: CA1480076888

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99594740T= , CM000666.2:g.99594740T=	GRCh38
NC_000004.11:g.100515897T= , CM000666.1:g.100515897T=	GRCh37
NC_000004.10:g.100734920T=	NCBI36
NG_011469.1:g.35658T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.766T= MANE Select	ENSP00000265517.5:p.Leu256=
ENST00000457717.6:c.766T=	ENSP00000400821.1:p.Leu256=
ENST00000511045.6:c.517T=	ENSP00000427679.2:p.Leu173=
ENST00000265517.9:c.766T=	ENSP00000265517.5:p.Leu256=
ENST00000457717.5:c.766T=	ENSP00000400821.1:p.Leu256=
ENST00000511045.5:c.847T=	ENSP00000427679.1:p.Leu283=
ENST00000619629.1:c.766T=	ENSP00000482850.1:p.Leu256=
NM_000253.3:c.766T=	NP_000244.2:p.Leu256=
NM_001300785.1:c.847T=	NP_001287714.1:p.Leu283=
NM_000253.4:c.766T=	NP_000244.2:p.Leu256=
NM_001300785.2:c.517T=	NP_001287714.2:p.Leu173=
NM_001386140.1:c.766T= MANE Select	NP_001373069.1:p.Leu256=