Canonical Allele Identifier: CA2583634792

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18869258_18869263dup , CM000681.2:g.18869258_18869263dup GRCh38
NC_000019.9:g.18980067_18980072dup , CM000681.1:g.18980067_18980072dup GRCh37
NC_000019.8:g.18841067_18841072dup NCBI36
NG_012070.1:g.31882_31887dup
NG_033056.1:g.31882_31887dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000623882.4:c.*722_*727dup (CERS1) MANE Select ENSP00000485308.1:n.*722_*727dup
ENST00000247005.8:c.453_458dup (GDF1) MANE Select ENSP00000247005.5:p.Ala153_Ala154insAlaAla
ENST00000247005.7:c.453_458dup (GDF1) ENSP00000247005.5:p.Ala153_Ala154insAlaAla
ENST00000623882.3:c.*722_*727dup (CERS1) ENSP00000485308.1:n.*722_*727dup
ENST00000623927.1:c.453_458dup (CERS1) ENSP00000485582.1:p.Ala153_Ala154insAlaAla
NM_001492.5:c.453_458dup (GDF1) NP_001483.3:p.Ala153_Ala154insAlaAla
NM_021267.4:c.*722_*727dup (CERS1) NP_067090.1:n.*722_*727dup
NM_001492.6:c.453_458dup (GDF1) MANE Select NP_001483.3:p.Ala153_Ala154insAlaAla
NM_021267.5:c.*722_*727dup (CERS1) MANE Select NP_067090.1:n.*722_*727dup
NM_001387438.1:c.453_458dup (GDF1) NP_001374367.1:p.Ala153_Ala154insAlaAla
NM_001387440.1:c.*1314_*1319dup (CERS1) NP_001374369.1:n.*1314_*1319dup