Canonical Allele Identifier: CA2578152542

Gene: MTTP

Linked Data

• gnomAD v4: 4-99622908-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622908A>G , CM000666.2:g.99622908A>G	GRCh38
NC_000004.11:g.100544065A>G , CM000666.1:g.100544065A>G	GRCh37
NC_000004.10:g.100763088A>G	NCBI36
NG_011469.1:g.63826A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.*60A>G MANE Select	ENSP00000265517.5:n.*60A>G
ENST00000457717.6:c.*60A>G	ENSP00000400821.1:n.*60A>G
ENST00000511045.6:c.*60A>G	ENSP00000427679.2:n.*60A>G
ENST00000265517.9:c.*60A>G	ENSP00000265517.5:n.*60A>G
ENST00000457717.5:c.*60A>G	ENSP00000400821.1:n.*60A>G
ENST00000511045.5:c.*60A>G	ENSP00000427679.1:n.*60A>G
ENST00000619629.1:c.*1192A>G	ENSP00000482850.1:n.*1192A>G
NM_000253.3:c.*60A>G	NP_000244.2:n.*60A>G
NM_001300785.1:c.*60A>G	NP_001287714.1:n.*60A>G
NM_000253.4:c.*60A>G	NP_000244.2:n.*60A>G
NM_001300785.2:c.*60A>G	NP_001287714.2:n.*60A>G
NM_001386140.1:c.*60A>G MANE Select	NP_001373069.1:n.*60A>G