Canonical Allele Identifier: CA1480066755

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583507T= , CM000666.2:g.99583507T=	GRCh38
NC_000004.11:g.100504664T= , CM000666.1:g.100504664T=	GRCh37
NC_000004.10:g.100723687T=	NCBI36
NG_011469.1:g.24425T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.383T= MANE Select	ENSP00000265517.5:p.Ile128=
ENST00000457717.6:c.383T=	ENSP00000400821.1:p.Ile128=
ENST00000511045.6:c.134T=	ENSP00000427679.2:p.Ile45=
ENST00000265517.9:c.383T=	ENSP00000265517.5:p.Ile128=
ENST00000422897.6:c.383T=	ENSP00000407350.2:p.Ile128=
ENST00000457717.5:c.383T=	ENSP00000400821.1:p.Ile128=
ENST00000506883.5:c.413T=	ENSP00000426755.1:p.Ile138=
ENST00000511045.5:c.464T=	ENSP00000427679.1:p.Ile155=
ENST00000619629.1:c.383T=	ENSP00000482850.1:p.Ile128=
NM_000253.3:c.383T=	NP_000244.2:p.Ile128=
NM_001300785.1:c.464T=	NP_001287714.1:p.Ile155=
NM_000253.4:c.383T=	NP_000244.2:p.Ile128=
NM_001300785.2:c.134T=	NP_001287714.2:p.Ile45=
NM_001386140.1:c.383T= MANE Select	NP_001373069.1:p.Ile128=