Canonical Allele Identifier: CA2052273184
Gene: MGAT4C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.86751376A= , CM000674.2:g.86751376A= GRCh38
NC_000012.11:g.87145153A= , CM000674.1:g.87145153A= GRCh37
NC_000012.10:g.85669284A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000548651.6:c.-261-24135T= ENSP00000447253.1:n.-261-24135T=
ENST00000621808.5:c.-381-24135T= ENSP00000478300.1:n.-381-24135T=
ENST00000551921.2:n.240-24135T=
ENST00000621808.4:c.-381-24135T= ENSP00000478300.1:n.-381-24135T=
NM_013244.3:c.-229+87290T= NP_037376.2:n.-229+87290T=
NM_001351285.1:c.-326-24135T= NP_001338214.1:n.-326-24135T=
NM_001351286.1:c.-261-24135T= NP_001338215.1:n.-261-24135T=
NM_013244.4:c.-229+87290T= NP_037376.2:n.-229+87290T=
NM_001351285.2:c.-326-24135T= NP_001338214.1:n.-326-24135T=
NM_001351286.2:c.-261-24135T= NP_001338215.1:n.-261-24135T=
NM_013244.5:c.-229+87290T= NP_037376.2:n.-229+87290T=