Canonical Allele Identifier: CA357520883

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100544000T>A (hg19) ; chr4:g.99622843T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622843T>A , CM000666.2:g.99622843T>A	GRCh38
NC_000004.11:g.100544000T>A , CM000666.1:g.100544000T>A	GRCh37
NC_000004.10:g.100763023T>A	NCBI36
NG_011469.1:g.63761T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2680T>A MANE Select	ENSP00000265517.5:p.Phe894Ile
ENST00000457717.6:c.2680T>A	ENSP00000400821.1:p.Phe894Ile
ENST00000511045.6:c.2431T>A	ENSP00000427679.2:p.Phe811Ile
ENST00000265517.9:c.2680T>A	ENSP00000265517.5:p.Phe894Ile
ENST00000457717.5:c.2680T>A	ENSP00000400821.1:p.Phe894Ile
ENST00000511045.5:c.2761T>A	ENSP00000427679.1:p.Phe921Ile
ENST00000619629.1:c.*1127T>A	ENSP00000482850.1:n.*1127T>A
NM_000253.3:c.2680T>A	NP_000244.2:p.Phe894Ile
NM_001300785.1:c.2761T>A	NP_001287714.1:p.Phe921Ile
NM_000253.4:c.2680T>A	NP_000244.2:p.Phe894Ile
NM_001300785.2:c.2431T>A	NP_001287714.2:p.Phe811Ile
NM_001386140.1:c.2680T>A MANE Select	NP_001373069.1:p.Phe894Ile