Canonical Allele Identifier: CA357505717

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100515927A>G (hg19) ; chr4:g.99594770A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99594770A>G , CM000666.2:g.99594770A>G	GRCh38
NC_000004.11:g.100515927A>G , CM000666.1:g.100515927A>G	GRCh37
NC_000004.10:g.100734950A>G	NCBI36
NG_011469.1:g.35688A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.796A>G MANE Select	ENSP00000265517.5:p.Arg266Gly
ENST00000457717.6:c.796A>G	ENSP00000400821.1:p.Arg266Gly
ENST00000511045.6:c.547A>G	ENSP00000427679.2:p.Arg183Gly
ENST00000265517.9:c.796A>G	ENSP00000265517.5:p.Arg266Gly
ENST00000457717.5:c.796A>G	ENSP00000400821.1:p.Arg266Gly
ENST00000511045.5:c.877A>G	ENSP00000427679.1:p.Arg293Gly
ENST00000619629.1:c.796A>G	ENSP00000482850.1:p.Arg266Gly
NM_000253.3:c.796A>G	NP_000244.2:p.Arg266Gly
NM_001300785.1:c.877A>G	NP_001287714.1:p.Arg293Gly
NM_000253.4:c.796A>G	NP_000244.2:p.Arg266Gly
NM_001300785.2:c.547A>G	NP_001287714.2:p.Arg183Gly
NM_001386140.1:c.796A>G MANE Select	NP_001373069.1:p.Arg266Gly