Canonical Allele Identifier: CA2052273318
Gene: MGAT4C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.86751543C= , CM000674.2:g.86751543C= GRCh38
NC_000012.11:g.87145320C= , CM000674.1:g.87145320C= GRCh37
NC_000012.10:g.85669451C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000548651.6:c.-261-24302G= ENSP00000447253.1:n.-261-24302G=
ENST00000621808.5:c.-381-24302G= ENSP00000478300.1:n.-381-24302G=
ENST00000551921.2:n.240-24302G=
ENST00000621808.4:c.-381-24302G= ENSP00000478300.1:n.-381-24302G=
NM_013244.3:c.-229+87123G= NP_037376.2:n.-229+87123G=
NM_001351285.1:c.-326-24302G= NP_001338214.1:n.-326-24302G=
NM_001351286.1:c.-261-24302G= NP_001338215.1:n.-261-24302G=
NM_013244.4:c.-229+87123G= NP_037376.2:n.-229+87123G=
NM_001351285.2:c.-326-24302G= NP_001338214.1:n.-326-24302G=
NM_001351286.2:c.-261-24302G= NP_001338215.1:n.-261-24302G=
NM_013244.5:c.-229+87123G= NP_037376.2:n.-229+87123G=