Canonical Allele Identifier: CA102649185

Gene: MTTP

Linked Data

• dbSNP Id: rs949986938
• MyVariant Identifiers: chr4:g.100539862T>C (hg19) ; chr4:g.99618705T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99618705T>C , CM000666.2:g.99618705T>C	GRCh38
NC_000004.11:g.100539862T>C , CM000666.1:g.100539862T>C	GRCh37
NC_000004.10:g.100758885T>C	NCBI36
NG_011469.1:g.59623T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.2218-269T>C MANE Select	ENSP00000265517.5:n.2218-269T>C
ENST00000457717.6:c.2218-269T>C	ENSP00000400821.1:n.2218-269T>C
ENST00000511045.6:c.1969-269T>C	ENSP00000427679.2:n.1969-269T>C
ENST00000265517.9:c.2218-269T>C	ENSP00000265517.5:n.2218-269T>C
ENST00000457717.5:c.2218-269T>C	ENSP00000400821.1:n.2218-269T>C
ENST00000511045.5:c.2299-269T>C	ENSP00000427679.1:n.2299-269T>C
ENST00000619629.1:c.*665-269T>C	ENSP00000482850.1:n.*665-269T>C
NM_000253.3:c.2218-269T>C	NP_000244.2:n.2218-269T>C
NM_001300785.1:c.2299-269T>C	NP_001287714.1:n.2299-269T>C
NM_000253.4:c.2218-269T>C	NP_000244.2:n.2218-269T>C
NM_001300785.2:c.1969-269T>C	NP_001287714.2:n.1969-269T>C
NM_001386140.1:c.2218-269T>C MANE Select	NP_001373069.1:n.2218-269T>C