Canonical Allele Identifier: CA357502126

Gene: MTTP

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583419A>T , CM000666.2:g.99583419A>T	GRCh38
NC_000004.11:g.100504576A>T , CM000666.1:g.100504576A>T	GRCh37
NC_000004.10:g.100723599A>T	NCBI36
NG_011469.1:g.24337A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.295A>T MANE Select	ENSP00000265517.5:p.Lys99Ter
ENST00000457717.6:c.295A>T	ENSP00000400821.1:p.Lys99Ter
ENST00000505094.6:c.46A>T	ENSP00000422782.2:p.Lys16Ter
ENST00000511045.6:c.46A>T	ENSP00000427679.2:p.Lys16Ter
ENST00000265517.9:c.295A>T	ENSP00000265517.5:p.Lys99Ter
ENST00000422897.6:c.295A>T	ENSP00000407350.2:p.Lys99Ter
ENST00000457717.5:c.295A>T	ENSP00000400821.1:p.Lys99Ter
ENST00000505094.5:c.*385A>T	ENSP00000422782.1:n.*385A>T
ENST00000506883.5:c.325A>T	ENSP00000426755.1:p.Lys109Ter
ENST00000511045.5:c.376A>T	ENSP00000427679.1:p.Lys126Ter
ENST00000515141.5:c.*358A>T	ENSP00000425642.1:n.*358A>T
ENST00000619629.1:c.295A>T	ENSP00000482850.1:p.Lys99Ter
NM_000253.3:c.295A>T	NP_000244.2:p.Lys99Ter
NM_001300785.1:c.376A>T	NP_001287714.1:p.Lys126Ter
NM_000253.4:c.295A>T	NP_000244.2:p.Lys99Ter
NM_001300785.2:c.46A>T	NP_001287714.2:p.Lys16Ter
NM_001386140.1:c.295A>T MANE Select	NP_001373069.1:p.Lys99Ter