Canonical Allele Identifier: CA3022046
Gene: MTTP HGNC NCBI

Linked Data

dbSNP Id: rs778024369

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99600707A>G , CM000666.2:g.99600707A>G GRCh38
NC_000004.11:g.100521864A>G , CM000666.1:g.100521864A>G GRCh37
NC_000004.10:g.100740887A>G NCBI36
NG_011469.1:g.41625A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.1210A>G MANE Select ENSP00000265517.5:p.Asn404Asp
ENST00000457717.6:c.1210A>G ENSP00000400821.1:p.Asn404Asp
ENST00000511045.6:c.961A>G ENSP00000427679.2:p.Asn321Asp
ENST00000265517.9:c.1210A>G ENSP00000265517.5:p.Asn404Asp
ENST00000457717.5:c.1210A>G ENSP00000400821.1:p.Asn404Asp
ENST00000511045.5:c.1291A>G ENSP00000427679.1:p.Asn431Asp
ENST00000619629.1:c.1210A>G ENSP00000482850.1:p.Asn404Asp
NM_000253.3:c.1210A>G NP_000244.2:p.Asn404Asp
NM_001300785.1:c.1291A>G NP_001287714.1:p.Asn431Asp
NM_000253.4:c.1210A>G NP_000244.2:p.Asn404Asp
NM_001300785.2:c.961A>G NP_001287714.2:p.Asn321Asp
NM_001386140.1:c.1210A>G MANE Select NP_001373069.1:p.Asn404Asp