Canonical Allele Identifier: CA1480088041

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622916C= , CM000666.2:g.99622916C=	GRCh38
NC_000004.11:g.100544073C= , CM000666.1:g.100544073C=	GRCh37
NC_000004.10:g.100763096C=	NCBI36
NG_011469.1:g.63834C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.*68C= MANE Select	ENSP00000265517.5:n.*68C=
ENST00000457717.6:c.*68C=	ENSP00000400821.1:n.*68C=
ENST00000511045.6:c.*68C=	ENSP00000427679.2:n.*68C=
ENST00000265517.9:c.*68C=	ENSP00000265517.5:n.*68C=
ENST00000457717.5:c.*68C=	ENSP00000400821.1:n.*68C=
ENST00000511045.5:c.*68C=	ENSP00000427679.1:n.*68C=
ENST00000619629.1:c.*1200C=	ENSP00000482850.1:n.*1200C=
NM_000253.3:c.*68C=	NP_000244.2:n.*68C=
NM_001300785.1:c.*68C=	NP_001287714.1:n.*68C=
NM_000253.4:c.*68C=	NP_000244.2:n.*68C=
NM_001300785.2:c.*68C=	NP_001287714.2:n.*68C=
NM_001386140.1:c.*68C= MANE Select	NP_001373069.1:n.*68C=