Canonical Allele Identifier: CA357520851

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100543995G>C (hg19) ; chr4:g.99622838G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622838G>C , CM000666.2:g.99622838G>C	GRCh38
NC_000004.11:g.100543995G>C , CM000666.1:g.100543995G>C	GRCh37
NC_000004.10:g.100763018G>C	NCBI36
NG_011469.1:g.63756G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2675G>C MANE Select	ENSP00000265517.5:p.Gly892Ala
ENST00000457717.6:c.2675G>C	ENSP00000400821.1:p.Gly892Ala
ENST00000511045.6:c.2426G>C	ENSP00000427679.2:p.Gly809Ala
ENST00000265517.9:c.2675G>C	ENSP00000265517.5:p.Gly892Ala
ENST00000457717.5:c.2675G>C	ENSP00000400821.1:p.Gly892Ala
ENST00000511045.5:c.2756G>C	ENSP00000427679.1:p.Gly919Ala
ENST00000619629.1:c.*1122G>C	ENSP00000482850.1:n.*1122G>C
NM_000253.3:c.2675G>C	NP_000244.2:p.Gly892Ala
NM_001300785.1:c.2756G>C	NP_001287714.1:p.Gly919Ala
NM_000253.4:c.2675G>C	NP_000244.2:p.Gly892Ala
NM_001300785.2:c.2426G>C	NP_001287714.2:p.Gly809Ala
NM_001386140.1:c.2675G>C MANE Select	NP_001373069.1:p.Gly892Ala