Canonical Allele Identifier: CA1480066703

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583420A= , CM000666.2:g.99583420A=	GRCh38
NC_000004.11:g.100504577A= , CM000666.1:g.100504577A=	GRCh37
NC_000004.10:g.100723600A=	NCBI36
NG_011469.1:g.24338A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.296A= MANE Select	ENSP00000265517.5:p.Lys99=
ENST00000457717.6:c.296A=	ENSP00000400821.1:p.Lys99=
ENST00000505094.6:c.47A=	ENSP00000422782.2:p.Lys16=
ENST00000511045.6:c.47A=	ENSP00000427679.2:p.Lys16=
ENST00000265517.9:c.296A=	ENSP00000265517.5:p.Lys99=
ENST00000422897.6:c.296A=	ENSP00000407350.2:p.Lys99=
ENST00000457717.5:c.296A=	ENSP00000400821.1:p.Lys99=
ENST00000505094.5:c.*386A=	ENSP00000422782.1:n.*386A=
ENST00000506883.5:c.326A=	ENSP00000426755.1:p.Lys109=
ENST00000511045.5:c.377A=	ENSP00000427679.1:p.Lys126=
ENST00000515141.5:c.*359A=	ENSP00000425642.1:n.*359A=
ENST00000619629.1:c.296A=	ENSP00000482850.1:p.Lys99=
NM_000253.3:c.296A=	NP_000244.2:p.Lys99=
NM_001300785.1:c.377A=	NP_001287714.1:p.Lys126=
NM_000253.4:c.296A=	NP_000244.2:p.Lys99=
NM_001300785.2:c.47A=	NP_001287714.2:p.Lys16=
NM_001386140.1:c.296A= MANE Select	NP_001373069.1:p.Lys99=