Canonical Allele Identifier: CA440328644

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100504650G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583493G>C , CM000666.2:g.99583493G>C	GRCh38
NC_000004.11:g.100504650G>C , CM000666.1:g.100504650G>C	GRCh37
NC_000004.10:g.100723673G>C	NCBI36
NG_011469.1:g.24411G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.369G>C MANE Select	ENSP00000265517.5:p.Thr123=
ENST00000457717.6:c.369G>C	ENSP00000400821.1:p.Thr123=
ENST00000511045.6:c.120G>C	ENSP00000427679.2:p.Thr40=
ENST00000265517.9:c.369G>C	ENSP00000265517.5:p.Thr123=
ENST00000422897.6:c.369G>C	ENSP00000407350.2:p.Thr123=
ENST00000457717.5:c.369G>C	ENSP00000400821.1:p.Thr123=
ENST00000506883.5:c.399G>C	ENSP00000426755.1:p.Thr133=
ENST00000511045.5:c.450G>C	ENSP00000427679.1:p.Thr150=
ENST00000619629.1:c.369G>C	ENSP00000482850.1:p.Thr123=
NM_000253.3:c.369G>C	NP_000244.2:p.Thr123=
NM_001300785.1:c.450G>C	NP_001287714.1:p.Thr150=
NM_000253.4:c.369G>C	NP_000244.2:p.Thr123=
NM_001300785.2:c.120G>C	NP_001287714.2:p.Thr40=
NM_001386140.1:c.369G>C MANE Select	NP_001373069.1:p.Thr123=