Canonical Allele Identifier: CA800747799

Gene: MTTP

Linked Data

• dbSNP Id: rs1195743185
• MyVariant Identifiers: chr4:g.100504850G>C (hg19) ; chr4:g.99583693G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583693G>C , CM000666.2:g.99583693G>C	GRCh38
NC_000004.11:g.100504850G>C , CM000666.1:g.100504850G>C	GRCh37
NC_000004.10:g.100723873G>C	NCBI36
NG_011469.1:g.24611G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+176G>C MANE Select	ENSP00000265517.5:n.393+176G>C
ENST00000457717.6:c.393+176G>C	ENSP00000400821.1:n.393+176G>C
ENST00000511045.6:c.144+176G>C	ENSP00000427679.2:n.144+176G>C
ENST00000265517.9:c.393+176G>C	ENSP00000265517.5:n.393+176G>C
ENST00000422897.6:c.*113G>C	ENSP00000407350.2:n.*113G>C
ENST00000457717.5:c.393+176G>C	ENSP00000400821.1:n.393+176G>C
ENST00000506883.5:c.423+176G>C	ENSP00000426755.1:n.423+176G>C
ENST00000511045.5:c.474+176G>C	ENSP00000427679.1:n.474+176G>C
ENST00000619629.1:c.393+176G>C	ENSP00000482850.1:n.393+176G>C
NM_000253.3:c.393+176G>C	NP_000244.2:n.393+176G>C
NM_001300785.1:c.474+176G>C	NP_001287714.1:n.474+176G>C
NM_000253.4:c.393+176G>C	NP_000244.2:n.393+176G>C
NM_001300785.2:c.144+176G>C	NP_001287714.2:n.144+176G>C
NM_001386140.1:c.393+176G>C MANE Select	NP_001373069.1:n.393+176G>C