Canonical Allele Identifier: CA440328662

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100504671A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583514A>T , CM000666.2:g.99583514A>T	GRCh38
NC_000004.11:g.100504671A>T , CM000666.1:g.100504671A>T	GRCh37
NC_000004.10:g.100723694A>T	NCBI36
NG_011469.1:g.24432A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.390A>T MANE Select	ENSP00000265517.5:p.Gly130=
ENST00000457717.6:c.390A>T	ENSP00000400821.1:p.Gly130=
ENST00000511045.6:c.141A>T	ENSP00000427679.2:p.Gly47=
ENST00000265517.9:c.390A>T	ENSP00000265517.5:p.Gly130=
ENST00000422897.6:c.390A>T	ENSP00000407350.2:p.Gly130=
ENST00000457717.5:c.390A>T	ENSP00000400821.1:p.Gly130=
ENST00000506883.5:c.420A>T	ENSP00000426755.1:p.Gly140=
ENST00000511045.5:c.471A>T	ENSP00000427679.1:p.Gly157=
ENST00000619629.1:c.390A>T	ENSP00000482850.1:p.Gly130=
NM_000253.3:c.390A>T	NP_000244.2:p.Gly130=
NM_001300785.1:c.471A>T	NP_001287714.1:p.Gly157=
NM_000253.4:c.390A>T	NP_000244.2:p.Gly130=
NM_001300785.2:c.141A>T	NP_001287714.2:p.Gly47=
NM_001386140.1:c.390A>T MANE Select	NP_001373069.1:p.Gly130=