Canonical Allele Identifier: CA1480079147

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600569C= , CM000666.2:g.99600569C=	GRCh38
NC_000004.11:g.100521726C= , CM000666.1:g.100521726C=	GRCh37
NC_000004.10:g.100740749C=	NCBI36
NG_011469.1:g.41487C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.1072C= MANE Select	ENSP00000265517.5:p.Gln358=
ENST00000457717.6:c.1072C=	ENSP00000400821.1:p.Gln358=
ENST00000511045.6:c.823C=	ENSP00000427679.2:p.Gln275=
ENST00000265517.9:c.1072C=	ENSP00000265517.5:p.Gln358=
ENST00000457717.5:c.1072C=	ENSP00000400821.1:p.Gln358=
ENST00000511045.5:c.1153C=	ENSP00000427679.1:p.Gln385=
ENST00000619629.1:c.1072C=	ENSP00000482850.1:p.Gln358=
NM_000253.3:c.1072C=	NP_000244.2:p.Gln358=
NM_001300785.1:c.1153C=	NP_001287714.1:p.Gln385=
NM_000253.4:c.1072C=	NP_000244.2:p.Gln358=
NM_001300785.2:c.823C=	NP_001287714.2:p.Gln275=
NM_001386140.1:c.1072C= MANE Select	NP_001373069.1:p.Gln358=