Canonical Allele Identifier: CA357520576

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100543948G>T (hg19) ; chr4:g.99622791G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622791G>T , CM000666.2:g.99622791G>T	GRCh38
NC_000004.11:g.100543948G>T , CM000666.1:g.100543948G>T	GRCh37
NC_000004.10:g.100762971G>T	NCBI36
NG_011469.1:g.63709G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2628G>T MANE Select	ENSP00000265517.5:p.Glu876Asp
ENST00000457717.6:c.2628G>T	ENSP00000400821.1:p.Glu876Asp
ENST00000511045.6:c.2379G>T	ENSP00000427679.2:p.Glu793Asp
ENST00000265517.9:c.2628G>T	ENSP00000265517.5:p.Glu876Asp
ENST00000457717.5:c.2628G>T	ENSP00000400821.1:p.Glu876Asp
ENST00000511045.5:c.2709G>T	ENSP00000427679.1:p.Glu903Asp
ENST00000619629.1:c.*1075G>T	ENSP00000482850.1:n.*1075G>T
NM_000253.3:c.2628G>T	NP_000244.2:p.Glu876Asp
NM_001300785.1:c.2709G>T	NP_001287714.1:p.Glu903Asp
NM_000253.4:c.2628G>T	NP_000244.2:p.Glu876Asp
NM_001300785.2:c.2379G>T	NP_001287714.2:p.Glu793Asp
NM_001386140.1:c.2628G>T MANE Select	NP_001373069.1:p.Glu876Asp