Canonical Allele Identifier: CA1480086513

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99619094A= , CM000666.2:g.99619094A=	GRCh38
NC_000004.11:g.100540251A= , CM000666.1:g.100540251A=	GRCh37
NC_000004.10:g.100759274A=	NCBI36
NG_011469.1:g.60012A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2338A= MANE Select	ENSP00000265517.5:p.Asn780=
ENST00000457717.6:c.2338A=	ENSP00000400821.1:p.Asn780=
ENST00000511045.6:c.2089A=	ENSP00000427679.2:p.Asn697=
ENST00000265517.9:c.2338A=	ENSP00000265517.5:p.Asn780=
ENST00000457717.5:c.2338A=	ENSP00000400821.1:p.Asn780=
ENST00000511045.5:c.2419A=	ENSP00000427679.1:p.Asn807=
ENST00000619629.1:c.*785A=	ENSP00000482850.1:n.*785A=
NM_000253.3:c.2338A=	NP_000244.2:p.Asn780=
NM_001300785.1:c.2419A=	NP_001287714.1:p.Asn807=
NM_000253.4:c.2338A=	NP_000244.2:p.Asn780=
NM_001300785.2:c.2089A=	NP_001287714.2:p.Asn697=
NM_001386140.1:c.2338A= MANE Select	NP_001373069.1:p.Asn780=