Canonical Allele Identifier: CA404862151

Gene: CERS1 GDF1

Linked Data

• gnomAD v4: 19-18868827-G-C
• MyVariant Identifiers: chr19:g.18979636G>C (hg19) ; chr19:g.18868827G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18868827G>C , CM000681.2:g.18868827G>C	GRCh38
NC_000019.9:g.18979636G>C , CM000681.1:g.18979636G>C	GRCh37
NC_000019.8:g.18840636G>C	NCBI36
NG_012070.1:g.32318C>G
NG_033056.1:g.32318C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000623882.4:c.*1158C>G (CERS1) MANE Select	ENSP00000485308.1:n.*1158C>G
ENST00000247005.8:c.889C>G (GDF1) MANE Select	ENSP00000247005.5:p.Gln297Glu
ENST00000247005.7:c.889C>G (GDF1)	ENSP00000247005.5:p.Gln297Glu
ENST00000623882.3:c.*1158C>G (CERS1)	ENSP00000485308.1:n.*1158C>G
ENST00000623927.1:c.889C>G (CERS1)	ENSP00000485582.1:p.Gln297Glu
NM_001492.5:c.889C>G (GDF1)	NP_001483.3:p.Gln297Glu
NM_021267.4:c.*1158C>G (CERS1)	NP_067090.1:n.*1158C>G
NM_001492.6:c.889C>G (GDF1) MANE Select	NP_001483.3:p.Gln297Glu
NM_021267.5:c.*1158C>G (CERS1) MANE Select	NP_067090.1:n.*1158C>G
NM_001387438.1:c.889C>G (GDF1)	NP_001374367.1:p.Gln297Glu
NM_001387440.1:c.*1750C>G (CERS1)	NP_001374369.1:n.*1750C>G