Canonical Allele Identifier: CA440328590

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100504548T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583391T>A , CM000666.2:g.99583391T>A	GRCh38
NC_000004.11:g.100504548T>A , CM000666.1:g.100504548T>A	GRCh37
NC_000004.10:g.100723571T>A	NCBI36
NG_011469.1:g.24309T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.267T>A MANE Select	ENSP00000265517.5:p.Val89=
ENST00000457717.6:c.267T>A	ENSP00000400821.1:p.Val89=
ENST00000505094.6:c.18T>A	ENSP00000422782.2:p.Val6=
ENST00000511045.6:c.18T>A	ENSP00000427679.2:p.Val6=
ENST00000265517.9:c.267T>A	ENSP00000265517.5:p.Val89=
ENST00000422897.6:c.267T>A	ENSP00000407350.2:p.Val89=
ENST00000457717.5:c.267T>A	ENSP00000400821.1:p.Val89=
ENST00000505094.5:c.*357T>A	ENSP00000422782.1:n.*357T>A
ENST00000506883.5:c.297T>A	ENSP00000426755.1:p.Val99=
ENST00000511045.5:c.348T>A	ENSP00000427679.1:p.Val116=
ENST00000513404.5:c.*330T>A	ENSP00000424972.1:n.*330T>A
ENST00000515141.5:c.*330T>A	ENSP00000425642.1:n.*330T>A
ENST00000619629.1:c.267T>A	ENSP00000482850.1:p.Val89=
NM_000253.3:c.267T>A	NP_000244.2:p.Val89=
NM_001300785.1:c.348T>A	NP_001287714.1:p.Val116=
NM_000253.4:c.267T>A	NP_000244.2:p.Val89=
NM_001300785.2:c.18T>A	NP_001287714.2:p.Val6=
NM_001386140.1:c.267T>A MANE Select	NP_001373069.1:p.Val89=