Canonical Allele Identifier: CA553130927
Gene: MTTP HGNC NCBI

Linked Data

dbSNP Id: rs1352300623
gnomAD v3: 4-99618728-A-G
gnomAD v4: 4-99618728-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99618728A>G , CM000666.2:g.99618728A>G GRCh38
NC_000004.11:g.100539885A>G , CM000666.1:g.100539885A>G GRCh37
NC_000004.10:g.100758908A>G NCBI36
NG_011469.1:g.59646A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.2218-246A>G MANE Select ENSP00000265517.5:n.2218-246A>G
ENST00000457717.6:c.2218-246A>G ENSP00000400821.1:n.2218-246A>G
ENST00000511045.6:c.1969-246A>G ENSP00000427679.2:n.1969-246A>G
ENST00000265517.9:c.2218-246A>G ENSP00000265517.5:n.2218-246A>G
ENST00000457717.5:c.2218-246A>G ENSP00000400821.1:n.2218-246A>G
ENST00000511045.5:c.2299-246A>G ENSP00000427679.1:n.2299-246A>G
ENST00000619629.1:c.*665-246A>G ENSP00000482850.1:n.*665-246A>G
NM_000253.3:c.2218-246A>G NP_000244.2:n.2218-246A>G
NM_001300785.1:c.2299-246A>G NP_001287714.1:n.2299-246A>G
NM_000253.4:c.2218-246A>G NP_000244.2:n.2218-246A>G
NM_001300785.2:c.1969-246A>G NP_001287714.2:n.1969-246A>G
NM_001386140.1:c.2218-246A>G MANE Select NP_001373069.1:n.2218-246A>G