Canonical Allele Identifier: CA1480079184

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600680T= , CM000666.2:g.99600680T=	GRCh38
NC_000004.11:g.100521837T= , CM000666.1:g.100521837T=	GRCh37
NC_000004.10:g.100740860T=	NCBI36
NG_011469.1:g.41598T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1183T= MANE Select	ENSP00000265517.5:p.Tyr395=
ENST00000457717.6:c.1183T=	ENSP00000400821.1:p.Tyr395=
ENST00000511045.6:c.934T=	ENSP00000427679.2:p.Tyr312=
ENST00000265517.9:c.1183T=	ENSP00000265517.5:p.Tyr395=
ENST00000457717.5:c.1183T=	ENSP00000400821.1:p.Tyr395=
ENST00000511045.5:c.1264T=	ENSP00000427679.1:p.Tyr422=
ENST00000619629.1:c.1183T=	ENSP00000482850.1:p.Tyr395=
NM_000253.3:c.1183T=	NP_000244.2:p.Tyr395=
NM_001300785.1:c.1264T=	NP_001287714.1:p.Tyr422=
NM_000253.4:c.1183T=	NP_000244.2:p.Tyr395=
NM_001300785.2:c.934T=	NP_001287714.2:p.Tyr312=
NM_001386140.1:c.1183T= MANE Select	NP_001373069.1:p.Tyr395=