Canonical Allele Identifier: CA2583634820

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18869404_18869405insGGG , CM000681.2:g.18869404_18869405insGGG GRCh38
NC_000019.9:g.18980213_18980214insGGG , CM000681.1:g.18980213_18980214insGGG GRCh37
NC_000019.8:g.18841213_18841214insGGG NCBI36
NG_012070.1:g.31740_31741insCCC
NG_033056.1:g.31740_31741insCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000623882.4:c.*595-15_*595-14insCCC (CERS1) MANE Select ENSP00000485308.1:n.*595-15_*595-14insCCC
ENST00000247005.8:c.326-15_326-14insCCC (GDF1) MANE Select ENSP00000247005.5:n.326-15_326-14insCCC
ENST00000247005.7:c.326-15_326-14insCCC (GDF1) ENSP00000247005.5:n.326-15_326-14insCCC
ENST00000623882.3:c.*595-15_*595-14insCCC (CERS1) ENSP00000485308.1:n.*595-15_*595-14insCCC
ENST00000623927.1:c.326-15_326-14insCCC (CERS1) ENSP00000485582.1:n.326-15_326-14insCCC
NM_001492.5:c.326-15_326-14insCCC (GDF1) NP_001483.3:n.326-15_326-14insCCC
NM_021267.4:c.*595-15_*595-14insCCC (CERS1) NP_067090.1:n.*595-15_*595-14insCCC
NM_001492.6:c.326-15_326-14insCCC (GDF1) MANE Select NP_001483.3:n.326-15_326-14insCCC
NM_021267.5:c.*595-15_*595-14insCCC (CERS1) MANE Select NP_067090.1:n.*595-15_*595-14insCCC
NM_001387438.1:c.326-15_326-14insCCC (GDF1) NP_001374367.1:n.326-15_326-14insCCC
NM_001387440.1:c.*1172_*1173insCCC (CERS1) NP_001374369.1:n.*1172_*1173insCCC