Canonical Allele Identifier: CA2052273232
Gene: MGAT4C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.86751445_86751448delinsCAAA , CM000674.2:g.86751445_86751448delinsCAAA GRCh38
NC_000012.11:g.87145222_87145225delinsCAAA , CM000674.1:g.87145222_87145225delinsCAAA GRCh37
NC_000012.10:g.85669353_85669356delinsCAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000548651.6:c.-261-24207_-261-24204delinsTTTG ENSP00000447253.1:n.-261-24207_-261-24204delinsTTTG
ENST00000621808.5:c.-381-24207_-381-24204delinsTTTG ENSP00000478300.1:n.-381-24207_-381-24204delinsTTTG
ENST00000551921.2:n.240-24207_240-24204delinsTTTG
ENST00000621808.4:c.-381-24207_-381-24204delinsTTTG ENSP00000478300.1:n.-381-24207_-381-24204delinsTTTG
NM_013244.3:c.-229+87218_-229+87221delinsTTTG NP_037376.2:n.-229+87218_-229+87221delinsTTTG
NM_001351285.1:c.-326-24207_-326-24204delinsTTTG NP_001338214.1:n.-326-24207_-326-24204delinsTTTG
NM_001351286.1:c.-261-24207_-261-24204delinsTTTG NP_001338215.1:n.-261-24207_-261-24204delinsTTTG
NM_013244.4:c.-229+87218_-229+87221delinsTTTG NP_037376.2:n.-229+87218_-229+87221delinsTTTG
NM_001351285.2:c.-326-24207_-326-24204delinsTTTG NP_001338214.1:n.-326-24207_-326-24204delinsTTTG
NM_001351286.2:c.-261-24207_-261-24204delinsTTTG NP_001338215.1:n.-261-24207_-261-24204delinsTTTG
NM_013244.5:c.-229+87218_-229+87221delinsTTTG NP_037376.2:n.-229+87218_-229+87221delinsTTTG