Canonical Allele Identifier: CA357502251

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100504604C>T (hg19) ; chr4:g.99583447C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583447C>T , CM000666.2:g.99583447C>T	GRCh38
NC_000004.11:g.100504604C>T , CM000666.1:g.100504604C>T	GRCh37
NC_000004.10:g.100723627C>T	NCBI36
NG_011469.1:g.24365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.323C>T MANE Select	ENSP00000265517.5:p.Ser108Phe
ENST00000457717.6:c.323C>T	ENSP00000400821.1:p.Ser108Phe
ENST00000511045.6:c.74C>T	ENSP00000427679.2:p.Ser25Phe
ENST00000265517.9:c.323C>T	ENSP00000265517.5:p.Ser108Phe
ENST00000422897.6:c.323C>T	ENSP00000407350.2:p.Ser108Phe
ENST00000457717.5:c.323C>T	ENSP00000400821.1:p.Ser108Phe
ENST00000506883.5:c.353C>T	ENSP00000426755.1:p.Ser118Phe
ENST00000511045.5:c.404C>T	ENSP00000427679.1:p.Ser135Phe
ENST00000515141.5:c.*386C>T	ENSP00000425642.1:n.*386C>T
ENST00000619629.1:c.323C>T	ENSP00000482850.1:p.Ser108Phe
NM_000253.3:c.323C>T	NP_000244.2:p.Ser108Phe
NM_001300785.1:c.404C>T	NP_001287714.1:p.Ser135Phe
NM_000253.4:c.323C>T	NP_000244.2:p.Ser108Phe
NM_001300785.2:c.74C>T	NP_001287714.2:p.Ser25Phe
NM_001386140.1:c.323C>T MANE Select	NP_001373069.1:p.Ser108Phe