Canonical Allele Identifier: CA357502128

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100504577A>T (hg19) ; chr4:g.99583420A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583420A>T , CM000666.2:g.99583420A>T	GRCh38
NC_000004.11:g.100504577A>T , CM000666.1:g.100504577A>T	GRCh37
NC_000004.10:g.100723600A>T	NCBI36
NG_011469.1:g.24338A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.296A>T MANE Select	ENSP00000265517.5:p.Lys99Met
ENST00000457717.6:c.296A>T	ENSP00000400821.1:p.Lys99Met
ENST00000505094.6:c.47A>T	ENSP00000422782.2:p.Lys16Met
ENST00000511045.6:c.47A>T	ENSP00000427679.2:p.Lys16Met
ENST00000265517.9:c.296A>T	ENSP00000265517.5:p.Lys99Met
ENST00000422897.6:c.296A>T	ENSP00000407350.2:p.Lys99Met
ENST00000457717.5:c.296A>T	ENSP00000400821.1:p.Lys99Met
ENST00000505094.5:c.*386A>T	ENSP00000422782.1:n.*386A>T
ENST00000506883.5:c.326A>T	ENSP00000426755.1:p.Lys109Met
ENST00000511045.5:c.377A>T	ENSP00000427679.1:p.Lys126Met
ENST00000515141.5:c.*359A>T	ENSP00000425642.1:n.*359A>T
ENST00000619629.1:c.296A>T	ENSP00000482850.1:p.Lys99Met
NM_000253.3:c.296A>T	NP_000244.2:p.Lys99Met
NM_001300785.1:c.377A>T	NP_001287714.1:p.Lys126Met
NM_000253.4:c.296A>T	NP_000244.2:p.Lys99Met
NM_001300785.2:c.47A>T	NP_001287714.2:p.Lys16Met
NM_001386140.1:c.296A>T MANE Select	NP_001373069.1:p.Lys99Met