Canonical Allele Identifier: CA357520891

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100544001T>G (hg19) ; chr4:g.99622844T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622844T>G , CM000666.2:g.99622844T>G	GRCh38
NC_000004.11:g.100544001T>G , CM000666.1:g.100544001T>G	GRCh37
NC_000004.10:g.100763024T>G	NCBI36
NG_011469.1:g.63762T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2681T>G MANE Select	ENSP00000265517.5:p.Phe894Cys
ENST00000457717.6:c.2681T>G	ENSP00000400821.1:p.Phe894Cys
ENST00000511045.6:c.2432T>G	ENSP00000427679.2:p.Phe811Cys
ENST00000265517.9:c.2681T>G	ENSP00000265517.5:p.Phe894Cys
ENST00000457717.5:c.2681T>G	ENSP00000400821.1:p.Phe894Cys
ENST00000511045.5:c.2762T>G	ENSP00000427679.1:p.Phe921Cys
ENST00000619629.1:c.*1128T>G	ENSP00000482850.1:n.*1128T>G
NM_000253.3:c.2681T>G	NP_000244.2:p.Phe894Cys
NM_001300785.1:c.2762T>G	NP_001287714.1:p.Phe921Cys
NM_000253.4:c.2681T>G	NP_000244.2:p.Phe894Cys
NM_001300785.2:c.2432T>G	NP_001287714.2:p.Phe811Cys
NM_001386140.1:c.2681T>G MANE Select	NP_001373069.1:p.Phe894Cys