Canonical Allele Identifier: CA357508603

Gene: MTTP

Linked Data

• MyVariant Identifiers: chr4:g.100521864A>C (hg19) ; chr4:g.99600707A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600707A>C , CM000666.2:g.99600707A>C	GRCh38
NC_000004.11:g.100521864A>C , CM000666.1:g.100521864A>C	GRCh37
NC_000004.10:g.100740887A>C	NCBI36
NG_011469.1:g.41625A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1210A>C MANE Select	ENSP00000265517.5:p.Asn404His
ENST00000457717.6:c.1210A>C	ENSP00000400821.1:p.Asn404His
ENST00000511045.6:c.961A>C	ENSP00000427679.2:p.Asn321His
ENST00000265517.9:c.1210A>C	ENSP00000265517.5:p.Asn404His
ENST00000457717.5:c.1210A>C	ENSP00000400821.1:p.Asn404His
ENST00000511045.5:c.1291A>C	ENSP00000427679.1:p.Asn431His
ENST00000619629.1:c.1210A>C	ENSP00000482850.1:p.Asn404His
NM_000253.3:c.1210A>C	NP_000244.2:p.Asn404His
NM_001300785.1:c.1291A>C	NP_001287714.1:p.Asn431His
NM_000253.4:c.1210A>C	NP_000244.2:p.Asn404His
NM_001300785.2:c.961A>C	NP_001287714.2:p.Asn321His
NM_001386140.1:c.1210A>C MANE Select	NP_001373069.1:p.Asn404His