Canonical Allele Identifier: CA10622070

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99564186C>G , CM000666.2:g.99564186C>G	GRCh38
NC_000004.11:g.100485343C>G , CM000666.1:g.100485343C>G	GRCh37
NC_000004.10:g.100704366C>G	NCBI36
NG_011469.1:g.5104C>G
NG_041774.1:g.4872G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000253.3:c.-153C>G	NP_000244.2:n.-153C>G
NM_000253.4:c.-153C>G	NP_000244.2:n.-153C>G
NM_001300785.1:c.91C>G	NP_001287714.1:p.Arg31Gly
NM_001300785.2:c.-240C>G	NP_001287714.2:n.-240C>G
ENST00000457717.5:c.-153C>G	ENSP00000400821.1:n.-153C>G
ENST00000457717.6:c.-153C>G	ENSP00000400821.1:n.-153C>G
ENST00000504724.1:c.91C>G	ENSP00000422667.1:p.Arg31Gly
ENST00000505094.5:c.91C>G	ENSP00000422782.1:p.Arg31Gly
ENST00000505094.6:c.-402C>G	ENSP00000422782.2:n.-402C>G
ENST00000505142.5:c.91+255C>G	ENSP00000425987.1:n.91+255C>G
ENST00000506883.5:c.91+255C>G	ENSP00000426755.1:n.91+255C>G
ENST00000511045.5:c.91C>G	ENSP00000427679.1:p.Arg31Gly
ENST00000511045.6:c.-240C>G	ENSP00000427679.2:n.-240C>G
ENST00000511610.5:c.91C>G	ENSP00000422178.1:p.Arg31Gly
ENST00000511610.6:c.-319C>G	ENSP00000422178.2:n.-319C>G
ENST00000513404.5:c.91+255C>G	ENSP00000424972.1:n.91+255C>G
ENST00000515141.5:c.91C>G	ENSP00000425642.1:p.Arg31Gly