Canonical Allele Identifier: CA3022003

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99597173C>T , CM000666.2:g.99597173C>T	GRCh38
NC_000004.11:g.100518330C>T , CM000666.1:g.100518330C>T	GRCh37
NC_000004.10:g.100737353C>T	NCBI36
NG_011469.1:g.38091C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1016C>T MANE Select	ENSP00000265517.5:p.Ala339Val
ENST00000457717.6:c.1016C>T	ENSP00000400821.1:p.Ala339Val
ENST00000511045.6:c.767C>T	ENSP00000427679.2:p.Ala256Val
ENST00000265517.9:c.1016C>T	ENSP00000265517.5:p.Ala339Val
ENST00000457717.5:c.1016C>T	ENSP00000400821.1:p.Ala339Val
ENST00000511045.5:c.1097C>T	ENSP00000427679.1:p.Ala366Val
ENST00000619629.1:c.1016C>T	ENSP00000482850.1:p.Ala339Val
NM_000253.3:c.1016C>T	NP_000244.2:p.Ala339Val
NM_001300785.1:c.1097C>T	NP_001287714.1:p.Ala366Val
NM_000253.4:c.1016C>T	NP_000244.2:p.Ala339Val
NM_001300785.2:c.767C>T	NP_001287714.2:p.Ala256Val
NM_001386140.1:c.1016C>T MANE Select	NP_001373069.1:p.Ala339Val