Canonical Allele Identifier: CA2671532909

Gene: MTTP

Linked Data

• gnomAD v4: 4-99583616-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583616T>A , CM000666.2:g.99583616T>A	GRCh38
NC_000004.11:g.100504773T>A , CM000666.1:g.100504773T>A	GRCh37
NC_000004.10:g.100723796T>A	NCBI36
NG_011469.1:g.24534T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+99T>A MANE Select	ENSP00000265517.5:n.393+99T>A
ENST00000457717.6:c.393+99T>A	ENSP00000400821.1:n.393+99T>A
ENST00000511045.6:c.144+99T>A	ENSP00000427679.2:n.144+99T>A
ENST00000265517.9:c.393+99T>A	ENSP00000265517.5:n.393+99T>A
ENST00000422897.6:c.*36T>A	ENSP00000407350.2:n.*36T>A
ENST00000457717.5:c.393+99T>A	ENSP00000400821.1:n.393+99T>A
ENST00000506883.5:c.423+99T>A	ENSP00000426755.1:n.423+99T>A
ENST00000511045.5:c.474+99T>A	ENSP00000427679.1:n.474+99T>A
ENST00000619629.1:c.393+99T>A	ENSP00000482850.1:n.393+99T>A
NM_000253.3:c.393+99T>A	NP_000244.2:n.393+99T>A
NM_001300785.1:c.474+99T>A	NP_001287714.1:n.474+99T>A
NM_000253.4:c.393+99T>A	NP_000244.2:n.393+99T>A
NM_001300785.2:c.144+99T>A	NP_001287714.2:n.144+99T>A
NM_001386140.1:c.393+99T>A MANE Select	NP_001373069.1:n.393+99T>A