Canonical Allele Identifier: CA2326567949

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18869477_18869478delinsCG , CM000681.2:g.18869477_18869478delinsCG GRCh38
NC_000019.9:g.18980286_18980287delinsCG , CM000681.1:g.18980286_18980287delinsCG GRCh37
NC_000019.8:g.18841286_18841287delinsCG NCBI36
NG_012070.1:g.31667_31668delinsCG
NG_033056.1:g.31667_31668delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000623882.4:c.*595-88_*595-87delinsCG (CERS1) MANE Select ENSP00000485308.1:n.*595-88_*595-87delinsCG
ENST00000247005.8:c.326-88_326-87delinsCG (GDF1) MANE Select ENSP00000247005.5:n.326-88_326-87delinsCG
ENST00000247005.7:c.326-88_326-87delinsCG (GDF1) ENSP00000247005.5:n.326-88_326-87delinsCG
ENST00000623882.3:c.*595-88_*595-87delinsCG (CERS1) ENSP00000485308.1:n.*595-88_*595-87delinsCG
ENST00000623927.1:c.326-88_326-87delinsCG (CERS1) ENSP00000485582.1:n.326-88_326-87delinsCG
NM_001492.5:c.326-88_326-87delinsCG (GDF1) NP_001483.3:n.326-88_326-87delinsCG
NM_021267.4:c.*595-88_*595-87delinsCG (CERS1) NP_067090.1:n.*595-88_*595-87delinsCG
NM_001492.6:c.326-88_326-87delinsCG (GDF1) MANE Select NP_001483.3:n.326-88_326-87delinsCG
NM_021267.5:c.*595-88_*595-87delinsCG (CERS1) MANE Select NP_067090.1:n.*595-88_*595-87delinsCG
NM_001387438.1:c.326-88_326-87delinsCG (GDF1) NP_001374367.1:n.326-88_326-87delinsCG
NM_001387440.1:c.*1099_*1100delinsCG (CERS1) NP_001374369.1:n.*1099_*1100delinsCG