Canonical Allele Identifier: CA440332985

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100543882C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622725C>G , CM000666.2:g.99622725C>G	GRCh38
NC_000004.11:g.100543882C>G , CM000666.1:g.100543882C>G	GRCh37
NC_000004.10:g.100762905C>G	NCBI36
NG_011469.1:g.63643C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2562C>G MANE Select	ENSP00000265517.5:p.Val854=
ENST00000457717.6:c.2562C>G	ENSP00000400821.1:p.Val854=
ENST00000511045.6:c.2313C>G	ENSP00000427679.2:p.Val771=
ENST00000265517.9:c.2562C>G	ENSP00000265517.5:p.Val854=
ENST00000457717.5:c.2562C>G	ENSP00000400821.1:p.Val854=
ENST00000511045.5:c.2643C>G	ENSP00000427679.1:p.Val881=
ENST00000619629.1:c.*1009C>G	ENSP00000482850.1:n.*1009C>G
NM_000253.3:c.2562C>G	NP_000244.2:p.Val854=
NM_001300785.1:c.2643C>G	NP_001287714.1:p.Val881=
NM_000253.4:c.2562C>G	NP_000244.2:p.Val854=
NM_001300785.2:c.2313C>G	NP_001287714.2:p.Val771=
NM_001386140.1:c.2562C>G MANE Select	NP_001373069.1:p.Val854=