Canonical Allele Identifier: CA357502050

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100504558A>T (hg19) ; chr4:g.99583401A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583401A>T , CM000666.2:g.99583401A>T	GRCh38
NC_000004.11:g.100504558A>T , CM000666.1:g.100504558A>T	GRCh37
NC_000004.10:g.100723581A>T	NCBI36
NG_011469.1:g.24319A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.277A>T MANE Select	ENSP00000265517.5:p.Asn93Tyr
ENST00000457717.6:c.277A>T	ENSP00000400821.1:p.Asn93Tyr
ENST00000505094.6:c.28A>T	ENSP00000422782.2:p.Asn10Tyr
ENST00000511045.6:c.28A>T	ENSP00000427679.2:p.Asn10Tyr
ENST00000265517.9:c.277A>T	ENSP00000265517.5:p.Asn93Tyr
ENST00000422897.6:c.277A>T	ENSP00000407350.2:p.Asn93Tyr
ENST00000457717.5:c.277A>T	ENSP00000400821.1:p.Asn93Tyr
ENST00000505094.5:c.*367A>T	ENSP00000422782.1:n.*367A>T
ENST00000506883.5:c.307A>T	ENSP00000426755.1:p.Asn103Tyr
ENST00000511045.5:c.358A>T	ENSP00000427679.1:p.Asn120Tyr
ENST00000513404.5:c.*340A>T	ENSP00000424972.1:n.*340A>T
ENST00000515141.5:c.*340A>T	ENSP00000425642.1:n.*340A>T
ENST00000619629.1:c.277A>T	ENSP00000482850.1:p.Asn93Tyr
NM_000253.3:c.277A>T	NP_000244.2:p.Asn93Tyr
NM_001300785.1:c.358A>T	NP_001287714.1:p.Asn120Tyr
NM_000253.4:c.277A>T	NP_000244.2:p.Asn93Tyr
NM_001300785.2:c.28A>T	NP_001287714.2:p.Asn10Tyr
NM_001386140.1:c.277A>T MANE Select	NP_001373069.1:p.Asn93Tyr