Canonical Allele Identifier: CA357518163
Gene: MTTP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99618998A>T , CM000666.2:g.99618998A>T GRCh38
NC_000004.11:g.100540155A>T , CM000666.1:g.100540155A>T GRCh37
NC_000004.10:g.100759178A>T NCBI36
NG_011469.1:g.59916A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.2242A>T MANE Select ENSP00000265517.5:p.Lys748Ter
ENST00000457717.6:c.2242A>T ENSP00000400821.1:p.Lys748Ter
ENST00000511045.6:c.1993A>T ENSP00000427679.2:p.Lys665Ter
ENST00000265517.9:c.2242A>T ENSP00000265517.5:p.Lys748Ter
ENST00000457717.5:c.2242A>T ENSP00000400821.1:p.Lys748Ter
ENST00000511045.5:c.2323A>T ENSP00000427679.1:p.Lys775Ter
ENST00000619629.1:c.*689A>T ENSP00000482850.1:n.*689A>T
NM_000253.3:c.2242A>T NP_000244.2:p.Lys748Ter
NM_001300785.1:c.2323A>T NP_001287714.1:p.Lys775Ter
NM_000253.4:c.2242A>T NP_000244.2:p.Lys748Ter
NM_001300785.2:c.1993A>T NP_001287714.2:p.Lys665Ter
NM_001386140.1:c.2242A>T MANE Select NP_001373069.1:p.Lys748Ter