Canonical Allele Identifier: CA1480066314

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583078C= , CM000666.2:g.99583078C=	GRCh38
NC_000004.11:g.100504235C= , CM000666.1:g.100504235C=	GRCh37
NC_000004.10:g.100723258C=	NCBI36
NG_011469.1:g.23996C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.250-296C= MANE Select	ENSP00000265517.5:n.250-296C=
ENST00000457717.6:c.250-296C=	ENSP00000400821.1:n.250-296C=
ENST00000505094.6:c.1-296C=	ENSP00000422782.2:n.1-296C=
ENST00000511045.6:c.1-296C=	ENSP00000427679.2:n.1-296C=
ENST00000265517.9:c.250-296C=	ENSP00000265517.5:n.250-296C=
ENST00000422897.6:c.250-296C=	ENSP00000407350.2:n.250-296C=
ENST00000457717.5:c.250-296C=	ENSP00000400821.1:n.250-296C=
ENST00000505094.5:c.*340-296C=	ENSP00000422782.1:n.*340-296C=
ENST00000506883.5:c.280-296C=	ENSP00000426755.1:n.280-296C=
ENST00000511045.5:c.331-296C=	ENSP00000427679.1:n.331-296C=
ENST00000513404.5:c.*313-296C=	ENSP00000424972.1:n.*313-296C=
ENST00000515141.5:c.*313-296C=	ENSP00000425642.1:n.*313-296C=
ENST00000619629.1:c.250-296C=	ENSP00000482850.1:n.250-296C=
NM_000253.3:c.250-296C=	NP_000244.2:n.250-296C=
NM_001300785.1:c.331-296C=	NP_001287714.1:n.331-296C=
NM_000253.4:c.250-296C=	NP_000244.2:n.250-296C=
NM_001300785.2:c.1-296C=	NP_001287714.2:n.1-296C=
NM_001386140.1:c.250-296C= MANE Select	NP_001373069.1:n.250-296C=