Canonical Allele Identifier: CA357502322

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100504620G>T (hg19) ; chr4:g.99583463G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583463G>T , CM000666.2:g.99583463G>T	GRCh38
NC_000004.11:g.100504620G>T , CM000666.1:g.100504620G>T	GRCh37
NC_000004.10:g.100723643G>T	NCBI36
NG_011469.1:g.24381G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.339G>T MANE Select	ENSP00000265517.5:p.Lys113Asn
ENST00000457717.6:c.339G>T	ENSP00000400821.1:p.Lys113Asn
ENST00000511045.6:c.90G>T	ENSP00000427679.2:p.Lys30Asn
ENST00000265517.9:c.339G>T	ENSP00000265517.5:p.Lys113Asn
ENST00000422897.6:c.339G>T	ENSP00000407350.2:p.Lys113Asn
ENST00000457717.5:c.339G>T	ENSP00000400821.1:p.Lys113Asn
ENST00000506883.5:c.369G>T	ENSP00000426755.1:p.Lys123Asn
ENST00000511045.5:c.420G>T	ENSP00000427679.1:p.Lys140Asn
ENST00000515141.5:c.*402G>T	ENSP00000425642.1:n.*402G>T
ENST00000619629.1:c.339G>T	ENSP00000482850.1:p.Lys113Asn
NM_000253.3:c.339G>T	NP_000244.2:p.Lys113Asn
NM_001300785.1:c.420G>T	NP_001287714.1:p.Lys140Asn
NM_000253.4:c.339G>T	NP_000244.2:p.Lys113Asn
NM_001300785.2:c.90G>T	NP_001287714.2:p.Lys30Asn
NM_001386140.1:c.339G>T MANE Select	NP_001373069.1:p.Lys113Asn