Canonical Allele Identifier: CA440333099

Gene: MTTP

Linked Data

• ClinVar Variation Id: 2699874
• ClinVar RCV Id: RCV003546976
• MyVariant Identifiers: chr4:g.100543915A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622758A>T , CM000666.2:g.99622758A>T	GRCh38
NC_000004.11:g.100543915A>T , CM000666.1:g.100543915A>T	GRCh37
NC_000004.10:g.100762938A>T	NCBI36
NG_011469.1:g.63676A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.2595A>T MANE Select	ENSP00000265517.5:p.Gly865=
ENST00000457717.6:c.2595A>T	ENSP00000400821.1:p.Gly865=
ENST00000511045.6:c.2346A>T	ENSP00000427679.2:p.Gly782=
ENST00000265517.9:c.2595A>T	ENSP00000265517.5:p.Gly865=
ENST00000457717.5:c.2595A>T	ENSP00000400821.1:p.Gly865=
ENST00000511045.5:c.2676A>T	ENSP00000427679.1:p.Gly892=
ENST00000619629.1:c.*1042A>T	ENSP00000482850.1:n.*1042A>T
NM_000253.3:c.2595A>T	NP_000244.2:p.Gly865=
NM_001300785.1:c.2676A>T	NP_001287714.1:p.Gly892=
NM_000253.4:c.2595A>T	NP_000244.2:p.Gly865=
NM_001300785.2:c.2346A>T	NP_001287714.2:p.Gly782=
NM_001386140.1:c.2595A>T MANE Select	NP_001373069.1:p.Gly865=