Canonical Allele Identifier: CA2671535539
Gene: MTTP HGNC NCBI

Linked Data

gnomAD v4: 4-99622660-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99622660T>A , CM000666.2:g.99622660T>A GRCh38
NC_000004.11:g.100543817T>A , CM000666.1:g.100543817T>A GRCh37
NC_000004.10:g.100762840T>A NCBI36
NG_011469.1:g.63578T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.2514-17T>A MANE Select ENSP00000265517.5:n.2514-17T>A
ENST00000457717.6:c.2514-17T>A ENSP00000400821.1:n.2514-17T>A
ENST00000511045.6:c.2265-17T>A ENSP00000427679.2:n.2265-17T>A
ENST00000265517.9:c.2514-17T>A ENSP00000265517.5:n.2514-17T>A
ENST00000457717.5:c.2514-17T>A ENSP00000400821.1:n.2514-17T>A
ENST00000511045.5:c.2595-17T>A ENSP00000427679.1:n.2595-17T>A
ENST00000619629.1:c.*961-17T>A ENSP00000482850.1:n.*961-17T>A
NM_000253.3:c.2514-17T>A NP_000244.2:n.2514-17T>A
NM_001300785.1:c.2595-17T>A NP_001287714.1:n.2595-17T>A
NM_000253.4:c.2514-17T>A NP_000244.2:n.2514-17T>A
NM_001300785.2:c.2265-17T>A NP_001287714.2:n.2265-17T>A
NM_001386140.1:c.2514-17T>A MANE Select NP_001373069.1:n.2514-17T>A
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