Canonical Allele Identifier: CA3021669

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99564098G>A , CM000666.2:g.99564098G>A	GRCh38
NC_000004.11:g.100485255G>A , CM000666.1:g.100485255G>A	GRCh37
NC_000004.10:g.100704278G>A	NCBI36
NG_011469.1:g.5016G>A
NG_041774.1:g.4960C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000253.3:c.-241G>A	NP_000244.2:n.-241G>A
NM_001300785.1:c.3G>A	NP_001287714.1:p.Met1Ile
ENST00000457717.5:c.-241G>A	ENSP00000400821.1:n.-241G>A
ENST00000457717.6:c.-241G>A	ENSP00000400821.1:n.-241G>A
ENST00000504724.1:c.3G>A	ENSP00000422667.1:p.Met1Ile
ENST00000505094.5:c.3G>A	ENSP00000422782.1:p.Met1Ile
ENST00000505094.6:c.-490G>A	ENSP00000422782.2:n.-490G>A
ENST00000505142.5:c.91+167G>A	ENSP00000425987.1:n.91+167G>A
ENST00000506883.5:c.91+167G>A	ENSP00000426755.1:n.91+167G>A
ENST00000511045.5:c.3G>A	ENSP00000427679.1:p.Met1Ile
ENST00000511045.6:c.-328G>A	ENSP00000427679.2:n.-328G>A
ENST00000511610.5:c.3G>A	ENSP00000422178.1:p.Met1Ile
ENST00000511610.6:c.-407G>A	ENSP00000422178.2:n.-407G>A
ENST00000513404.5:c.91+167G>A	ENSP00000424972.1:n.91+167G>A
ENST00000515141.5:c.3G>A	ENSP00000425642.1:p.Met1Ile