Canonical Allele Identifier: CA1480087971
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99622756G= , CM000666.2:g.99622756G= GRCh38
NC_000004.11:g.100543913G= , CM000666.1:g.100543913G= GRCh37
NC_000004.10:g.100762936G= NCBI36
NG_011469.1:g.63674G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.2593G= MANE Select ENSP00000265517.5:p.Gly865=
ENST00000457717.6:c.2593G= ENSP00000400821.1:p.Gly865=
ENST00000511045.6:c.2344G= ENSP00000427679.2:p.Gly782=
ENST00000265517.9:c.2593G= ENSP00000265517.5:p.Gly865=
ENST00000457717.5:c.2593G= ENSP00000400821.1:p.Gly865=
ENST00000511045.5:c.2674G= ENSP00000427679.1:p.Gly892=
ENST00000619629.1:c.*1040G= ENSP00000482850.1:n.*1040G=
NM_000253.3:c.2593G= NP_000244.2:p.Gly865=
NM_001300785.1:c.2674G= NP_001287714.1:p.Gly892=
NM_000253.4:c.2593G= NP_000244.2:p.Gly865=
NM_001300785.2:c.2344G= NP_001287714.2:p.Gly782=
NM_001386140.1:c.2593G= MANE Select NP_001373069.1:p.Gly865=