Canonical Allele Identifier: CA1480079174

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600656A= , CM000666.2:g.99600656A=	GRCh38
NC_000004.11:g.100521813A= , CM000666.1:g.100521813A=	GRCh37
NC_000004.10:g.100740836A=	NCBI36
NG_011469.1:g.41574A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1159A= MANE Select	ENSP00000265517.5:p.Ile387=
ENST00000457717.6:c.1159A=	ENSP00000400821.1:p.Ile387=
ENST00000511045.6:c.910A=	ENSP00000427679.2:p.Ile304=
ENST00000265517.9:c.1159A=	ENSP00000265517.5:p.Ile387=
ENST00000457717.5:c.1159A=	ENSP00000400821.1:p.Ile387=
ENST00000511045.5:c.1240A=	ENSP00000427679.1:p.Ile414=
ENST00000619629.1:c.1159A=	ENSP00000482850.1:p.Ile387=
NM_000253.3:c.1159A=	NP_000244.2:p.Ile387=
NM_001300785.1:c.1240A=	NP_001287714.1:p.Ile414=
NM_000253.4:c.1159A=	NP_000244.2:p.Ile387=
NM_001300785.2:c.910A=	NP_001287714.2:p.Ile304=
NM_001386140.1:c.1159A= MANE Select	NP_001373069.1:p.Ile387=