Canonical Allele Identifier: CA440328658
Gene: MTTP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100504665C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99583508C>T , CM000666.2:g.99583508C>T GRCh38
NC_000004.11:g.100504665C>T , CM000666.1:g.100504665C>T GRCh37
NC_000004.10:g.100723688C>T NCBI36
NG_011469.1:g.24426C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.384C>T MANE Select ENSP00000265517.5:p.Ile128=
ENST00000457717.6:c.384C>T ENSP00000400821.1:p.Ile128=
ENST00000511045.6:c.135C>T ENSP00000427679.2:p.Ile45=
ENST00000265517.9:c.384C>T ENSP00000265517.5:p.Ile128=
ENST00000422897.6:c.384C>T ENSP00000407350.2:p.Ile128=
ENST00000457717.5:c.384C>T ENSP00000400821.1:p.Ile128=
ENST00000506883.5:c.414C>T ENSP00000426755.1:p.Ile138=
ENST00000511045.5:c.465C>T ENSP00000427679.1:p.Ile155=
ENST00000619629.1:c.384C>T ENSP00000482850.1:p.Ile128=
NM_000253.3:c.384C>T NP_000244.2:p.Ile128=
NM_001300785.1:c.465C>T NP_001287714.1:p.Ile155=
NM_000253.4:c.384C>T NP_000244.2:p.Ile128=
NM_001300785.2:c.135C>T NP_001287714.2:p.Ile45=
NM_001386140.1:c.384C>T MANE Select NP_001373069.1:p.Ile128=