Canonical Allele Identifier: CA1480066737

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583460A= , CM000666.2:g.99583460A=	GRCh38
NC_000004.11:g.100504617A= , CM000666.1:g.100504617A=	GRCh37
NC_000004.10:g.100723640A=	NCBI36
NG_011469.1:g.24378A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.336A= MANE Select	ENSP00000265517.5:p.Gly112=
ENST00000457717.6:c.336A=	ENSP00000400821.1:p.Gly112=
ENST00000511045.6:c.87A=	ENSP00000427679.2:p.Gly29=
ENST00000265517.9:c.336A=	ENSP00000265517.5:p.Gly112=
ENST00000422897.6:c.336A=	ENSP00000407350.2:p.Gly112=
ENST00000457717.5:c.336A=	ENSP00000400821.1:p.Gly112=
ENST00000506883.5:c.366A=	ENSP00000426755.1:p.Gly122=
ENST00000511045.5:c.417A=	ENSP00000427679.1:p.Gly139=
ENST00000515141.5:c.*399A=	ENSP00000425642.1:n.*399A=
ENST00000619629.1:c.336A=	ENSP00000482850.1:p.Gly112=
NM_000253.3:c.336A=	NP_000244.2:p.Gly112=
NM_001300785.1:c.417A=	NP_001287714.1:p.Gly139=
NM_000253.4:c.336A=	NP_000244.2:p.Gly112=
NM_001300785.2:c.87A=	NP_001287714.2:p.Gly29=
NM_001386140.1:c.336A= MANE Select	NP_001373069.1:p.Gly112=