Canonical Allele Identifier: CA1480087952

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622709C= , CM000666.2:g.99622709C=	GRCh38
NC_000004.11:g.100543866C= , CM000666.1:g.100543866C=	GRCh37
NC_000004.10:g.100762889C=	NCBI36
NG_011469.1:g.63627C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2546C= MANE Select	ENSP00000265517.5:p.Thr849=
ENST00000457717.6:c.2546C=	ENSP00000400821.1:p.Thr849=
ENST00000511045.6:c.2297C=	ENSP00000427679.2:p.Thr766=
ENST00000265517.9:c.2546C=	ENSP00000265517.5:p.Thr849=
ENST00000457717.5:c.2546C=	ENSP00000400821.1:p.Thr849=
ENST00000511045.5:c.2627C=	ENSP00000427679.1:p.Thr876=
ENST00000619629.1:c.*993C=	ENSP00000482850.1:n.*993C=
NM_000253.3:c.2546C=	NP_000244.2:p.Thr849=
NM_001300785.1:c.2627C=	NP_001287714.1:p.Thr876=
NM_000253.4:c.2546C=	NP_000244.2:p.Thr849=
NM_001300785.2:c.2297C=	NP_001287714.2:p.Thr766=
NM_001386140.1:c.2546C= MANE Select	NP_001373069.1:p.Thr849=