Canonical Allele Identifier: CA440328609
Gene: MTTP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100504590A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99583433A>G , CM000666.2:g.99583433A>G GRCh38
NC_000004.11:g.100504590A>G , CM000666.1:g.100504590A>G GRCh37
NC_000004.10:g.100723613A>G NCBI36
NG_011469.1:g.24351A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.309A>G MANE Select ENSP00000265517.5:p.Lys103=
ENST00000457717.6:c.309A>G ENSP00000400821.1:p.Lys103=
ENST00000511045.6:c.60A>G ENSP00000427679.2:p.Lys20=
ENST00000265517.9:c.309A>G ENSP00000265517.5:p.Lys103=
ENST00000422897.6:c.309A>G ENSP00000407350.2:p.Lys103=
ENST00000457717.5:c.309A>G ENSP00000400821.1:p.Lys103=
ENST00000506883.5:c.339A>G ENSP00000426755.1:p.Lys113=
ENST00000511045.5:c.390A>G ENSP00000427679.1:p.Lys130=
ENST00000515141.5:c.*372A>G ENSP00000425642.1:n.*372A>G
ENST00000619629.1:c.309A>G ENSP00000482850.1:p.Lys103=
NM_000253.3:c.309A>G NP_000244.2:p.Lys103=
NM_001300785.1:c.390A>G NP_001287714.1:p.Lys130=
NM_000253.4:c.309A>G NP_000244.2:p.Lys103=
NM_001300785.2:c.60A>G NP_001287714.2:p.Lys20=
NM_001386140.1:c.309A>G MANE Select NP_001373069.1:p.Lys103=