Canonical Allele Identifier: CA1480076819

Gene: MTTP

Linked Data

• dbSNP Id: rs1725504650

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99594581_99594582insCA , CM000666.2:g.99594581_99594582insCA	GRCh38
NC_000004.11:g.100515738_100515739insCA , CM000666.1:g.100515738_100515739insCA	GRCh37
NC_000004.10:g.100734761_100734762insCA	NCBI36
NG_011469.1:g.35499_35500insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.759-152_759-151insCA MANE Select	ENSP00000265517.5:n.759-152_759-151insCA
ENST00000457717.6:c.759-152_759-151insCA	ENSP00000400821.1:n.759-152_759-151insCA
ENST00000511045.6:c.510-152_510-151insCA	ENSP00000427679.2:n.510-152_510-151insCA
ENST00000265517.9:c.759-152_759-151insCA	ENSP00000265517.5:n.759-152_759-151insCA
ENST00000457717.5:c.759-152_759-151insCA	ENSP00000400821.1:n.759-152_759-151insCA
ENST00000511045.5:c.840-152_840-151insCA	ENSP00000427679.1:n.840-152_840-151insCA
ENST00000619629.1:c.759-152_759-151insCA	ENSP00000482850.1:n.759-152_759-151insCA
NM_000253.3:c.759-152_759-151insCA	NP_000244.2:n.759-152_759-151insCA
NM_001300785.1:c.840-152_840-151insCA	NP_001287714.1:n.840-152_840-151insCA
NM_000253.4:c.759-152_759-151insCA	NP_000244.2:n.759-152_759-151insCA
NM_001300785.2:c.510-152_510-151insCA	NP_001287714.2:n.510-152_510-151insCA
NM_001386140.1:c.759-152_759-151insCA MANE Select	NP_001373069.1:n.759-152_759-151insCA