Canonical Allele Identifier: CA1480072745

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99589746A= , CM000666.2:g.99589746A=	GRCh38
NC_000004.11:g.100510903A= , CM000666.1:g.100510903A=	GRCh37
NC_000004.10:g.100729926A=	NCBI36
NG_011469.1:g.30664A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.497A= MANE Select	ENSP00000265517.5:p.Asn166=
ENST00000457717.6:c.497A=	ENSP00000400821.1:p.Asn166=
ENST00000511045.6:c.248A=	ENSP00000427679.2:p.Asn83=
ENST00000265517.9:c.497A=	ENSP00000265517.5:p.Asn166=
ENST00000457717.5:c.497A=	ENSP00000400821.1:p.Asn166=
ENST00000506883.5:c.527A=	ENSP00000426755.1:p.Asn176=
ENST00000511045.5:c.578A=	ENSP00000427679.1:p.Asn193=
ENST00000619629.1:c.497A=	ENSP00000482850.1:p.Asn166=
NM_000253.3:c.497A=	NP_000244.2:p.Asn166=
NM_001300785.1:c.578A=	NP_001287714.1:p.Asn193=
NM_000253.4:c.497A=	NP_000244.2:p.Asn166=
NM_001300785.2:c.248A=	NP_001287714.2:p.Asn83=
NM_001386140.1:c.497A= MANE Select	NP_001373069.1:p.Asn166=