Canonical Allele Identifier: CA950115175
Gene: MGAT4C HGNC NCBI

Linked Data

dbSNP Id: rs1951228168

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.86751279del , CM000674.2:g.86751279del GRCh38
NC_000012.11:g.87145056del , CM000674.1:g.87145056del GRCh37
NC_000012.10:g.85669187del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000548651.6:c.-261-24038del ENSP00000447253.1:n.-261-24038del
ENST00000621808.5:c.-381-24038del ENSP00000478300.1:n.-381-24038del
ENST00000551921.2:n.240-24038del
ENST00000621808.4:c.-381-24038del ENSP00000478300.1:n.-381-24038del
NM_013244.3:c.-229+87387del NP_037376.2:n.-229+87387del
NM_001351285.1:c.-326-24038del NP_001338214.1:n.-326-24038del
NM_001351286.1:c.-261-24038del NP_001338215.1:n.-261-24038del
NM_013244.4:c.-229+87387del NP_037376.2:n.-229+87387del
NM_001351285.2:c.-326-24038del NP_001338214.1:n.-326-24038del
NM_001351286.2:c.-261-24038del NP_001338215.1:n.-261-24038del
NM_013244.5:c.-229+87387del NP_037376.2:n.-229+87387del