Canonical Allele Identifier: CA440332807

Gene: MTTP

Linked Data

• gnomAD v4: 4-99622677-G-A
• MyVariant Identifiers: chr4:g.100543834G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622677G>A , CM000666.2:g.99622677G>A	GRCh38
NC_000004.11:g.100543834G>A , CM000666.1:g.100543834G>A	GRCh37
NC_000004.10:g.100762857G>A	NCBI36
NG_011469.1:g.63595G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2514G>A MANE Select	ENSP00000265517.5:p.Arg838=
ENST00000457717.6:c.2514G>A	ENSP00000400821.1:p.Arg838=
ENST00000511045.6:c.2265G>A	ENSP00000427679.2:p.Arg755=
ENST00000265517.9:c.2514G>A	ENSP00000265517.5:p.Arg838=
ENST00000457717.5:c.2514G>A	ENSP00000400821.1:p.Arg838=
ENST00000511045.5:c.2595G>A	ENSP00000427679.1:p.Arg865=
ENST00000619629.1:c.*961G>A	ENSP00000482850.1:n.*961G>A
NM_000253.3:c.2514G>A	NP_000244.2:p.Arg838=
NM_001300785.1:c.2595G>A	NP_001287714.1:p.Arg865=
NM_000253.4:c.2514G>A	NP_000244.2:p.Arg838=
NM_001300785.2:c.2265G>A	NP_001287714.2:p.Arg755=
NM_001386140.1:c.2514G>A MANE Select	NP_001373069.1:p.Arg838=