Canonical Allele Identifier: CA2583634778

Gene: CERS1 GDF1

Linked Data

• gnomAD v4: 19-18869181-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18869185dup , CM000681.2:g.18869185dup	GRCh38
NC_000019.9:g.18979994dup , CM000681.1:g.18979994dup	GRCh37
NC_000019.8:g.18840994dup	NCBI36
NG_012070.1:g.31963dup
NG_033056.1:g.31963dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623882.4:c.*803dup (CERS1) MANE Select	ENSP00000485308.1:n.*803dup
ENST00000247005.8:c.534dup (GDF1) MANE Select	ENSP00000247005.5:p.Gly179ArgfsTer?
ENST00000247005.7:c.534dup (GDF1)	ENSP00000247005.5:p.Gly179ArgfsTer?
ENST00000623882.3:c.*803dup (CERS1)	ENSP00000485308.1:n.*803dup
ENST00000623927.1:c.534dup (CERS1)	ENSP00000485582.1:p.Gly179ArgfsTer?
NM_001492.5:c.534dup (GDF1)	NP_001483.3:p.Gly179ArgfsTer?
NM_021267.4:c.*803dup (CERS1)	NP_067090.1:n.*803dup
NM_001492.6:c.534dup (GDF1) MANE Select	NP_001483.3:p.Gly179ArgfsTer?
NM_021267.5:c.*803dup (CERS1) MANE Select	NP_067090.1:n.*803dup
NM_001387438.1:c.534dup (GDF1)	NP_001374367.1:p.Gly179ArgfsTer?
NM_001387440.1:c.*1395dup (CERS1)	NP_001374369.1:n.*1395dup