Canonical Allele Identifier: CA1480076817

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99594579C= , CM000666.2:g.99594579C=	GRCh38
NC_000004.11:g.100515736C= , CM000666.1:g.100515736C=	GRCh37
NC_000004.10:g.100734759C=	NCBI36
NG_011469.1:g.35497C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.759-154C= MANE Select	ENSP00000265517.5:n.759-154C=
ENST00000457717.6:c.759-154C=	ENSP00000400821.1:n.759-154C=
ENST00000511045.6:c.510-154C=	ENSP00000427679.2:n.510-154C=
ENST00000265517.9:c.759-154C=	ENSP00000265517.5:n.759-154C=
ENST00000457717.5:c.759-154C=	ENSP00000400821.1:n.759-154C=
ENST00000511045.5:c.840-154C=	ENSP00000427679.1:n.840-154C=
ENST00000619629.1:c.759-154C=	ENSP00000482850.1:n.759-154C=
NM_000253.3:c.759-154C=	NP_000244.2:n.759-154C=
NM_001300785.1:c.840-154C=	NP_001287714.1:n.840-154C=
NM_000253.4:c.759-154C=	NP_000244.2:n.759-154C=
NM_001300785.2:c.510-154C=	NP_001287714.2:n.510-154C=
NM_001386140.1:c.759-154C= MANE Select	NP_001373069.1:n.759-154C=