Canonical Allele Identifier: CA102652458

Gene: MTTP

Linked Data

• ClinVar Variation Id: 1209583
• ClinVar RCV Id: RCV001578628
• dbSNP Id: rs774949603
• gnomAD v2: 4-100543994-G-A
• gnomAD v3: 4-99622837-G-A
• gnomAD v4: 4-99622837-G-A
• MyVariant Identifiers: chr4:g.100543994G>A (hg19) ; chr4:g.99622837G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622837G>A , CM000666.2:g.99622837G>A	GRCh38
NC_000004.11:g.100543994G>A , CM000666.1:g.100543994G>A	GRCh37
NC_000004.10:g.100763017G>A	NCBI36
NG_011469.1:g.63755G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2674G>A MANE Select	ENSP00000265517.5:p.Gly892Arg
ENST00000457717.6:c.2674G>A	ENSP00000400821.1:p.Gly892Arg
ENST00000511045.6:c.2425G>A	ENSP00000427679.2:p.Gly809Arg
ENST00000265517.9:c.2674G>A	ENSP00000265517.5:p.Gly892Arg
ENST00000457717.5:c.2674G>A	ENSP00000400821.1:p.Gly892Arg
ENST00000511045.5:c.2755G>A	ENSP00000427679.1:p.Gly919Arg
ENST00000619629.1:c.*1121G>A	ENSP00000482850.1:n.*1121G>A
NM_000253.3:c.2674G>A	NP_000244.2:p.Gly892Arg
NM_001300785.1:c.2755G>A	NP_001287714.1:p.Gly919Arg
NM_000253.4:c.2674G>A	NP_000244.2:p.Gly892Arg
NM_001300785.2:c.2425G>A	NP_001287714.2:p.Gly809Arg
NM_001386140.1:c.2674G>A MANE Select	NP_001373069.1:p.Gly892Arg