Canonical Allele Identifier: CA1480087982

Gene: MTTP

Linked Data

• dbSNP Id: rs1726271635

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622780_99622781insTTACTG , CM000666.2:g.99622780_99622781insTTACTG	GRCh38
NC_000004.11:g.100543937_100543938insTTACTG , CM000666.1:g.100543937_100543938insTTACTG	GRCh37
NC_000004.10:g.100762960_100762961insTTACTG	NCBI36
NG_011469.1:g.63698_63699insTTACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2617_2618insTTACTG MANE Select	ENSP00000265517.5:p.Gln872_Glu873insValThr
ENST00000457717.6:c.2617_2618insTTACTG	ENSP00000400821.1:p.Gln872_Glu873insValThr
ENST00000511045.6:c.2368_2369insTTACTG	ENSP00000427679.2:p.Gln789_Glu790insValThr
ENST00000265517.9:c.2617_2618insTTACTG	ENSP00000265517.5:p.Gln872_Glu873insValThr
ENST00000457717.5:c.2617_2618insTTACTG	ENSP00000400821.1:p.Gln872_Glu873insValThr
ENST00000511045.5:c.2698_2699insTTACTG	ENSP00000427679.1:p.Gln899_Glu900insValThr
ENST00000619629.1:c.*1064_*1065insTTACTG	ENSP00000482850.1:n.*1064_*1065insTTACTG
NM_000253.3:c.2617_2618insTTACTG	NP_000244.2:p.Gln872_Glu873insValThr
NM_001300785.1:c.2698_2699insTTACTG	NP_001287714.1:p.Gln899_Glu900insValThr
NM_000253.4:c.2617_2618insTTACTG	NP_000244.2:p.Gln872_Glu873insValThr
NM_001300785.2:c.2368_2369insTTACTG	NP_001287714.2:p.Gln789_Glu790insValThr
NM_001386140.1:c.2617_2618insTTACTG MANE Select	NP_001373069.1:p.Gln872_Glu873insValThr