Canonical Allele Identifier: CA2052273186
Gene: MGAT4C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.86751381A= , CM000674.2:g.86751381A= GRCh38
NC_000012.11:g.87145158A= , CM000674.1:g.87145158A= GRCh37
NC_000012.10:g.85669289A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000548651.6:c.-261-24140T= ENSP00000447253.1:n.-261-24140T=
ENST00000621808.5:c.-381-24140T= ENSP00000478300.1:n.-381-24140T=
ENST00000551921.2:n.240-24140T=
ENST00000621808.4:c.-381-24140T= ENSP00000478300.1:n.-381-24140T=
NM_013244.3:c.-229+87285T= NP_037376.2:n.-229+87285T=
NM_001351285.1:c.-326-24140T= NP_001338214.1:n.-326-24140T=
NM_001351286.1:c.-261-24140T= NP_001338215.1:n.-261-24140T=
NM_013244.4:c.-229+87285T= NP_037376.2:n.-229+87285T=
NM_001351285.2:c.-326-24140T= NP_001338214.1:n.-326-24140T=
NM_001351286.2:c.-261-24140T= NP_001338215.1:n.-261-24140T=
NM_013244.5:c.-229+87285T= NP_037376.2:n.-229+87285T=
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