Canonical Allele Identifier: CA2583634809

Gene: CERS1 GDF1

Linked Data

• gnomAD v4: 19-18869397-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18869397A>C , CM000681.2:g.18869397A>C	GRCh38
NC_000019.9:g.18980206A>C , CM000681.1:g.18980206A>C	GRCh37
NC_000019.8:g.18841206A>C	NCBI36
NG_012070.1:g.31748T>G
NG_033056.1:g.31748T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623882.4:c.*595-7T>G (CERS1) MANE Select	ENSP00000485308.1:n.*595-7T>G
ENST00000247005.8:c.326-7T>G (GDF1) MANE Select	ENSP00000247005.5:n.326-7T>G
ENST00000247005.7:c.326-7T>G (GDF1)	ENSP00000247005.5:n.326-7T>G
ENST00000623882.3:c.*595-7T>G (CERS1)	ENSP00000485308.1:n.*595-7T>G
ENST00000623927.1:c.326-7T>G (CERS1)	ENSP00000485582.1:n.326-7T>G
NM_001492.5:c.326-7T>G (GDF1)	NP_001483.3:n.326-7T>G
NM_021267.4:c.*595-7T>G (CERS1)	NP_067090.1:n.*595-7T>G
NM_001492.6:c.326-7T>G (GDF1) MANE Select	NP_001483.3:n.326-7T>G
NM_021267.5:c.*595-7T>G (CERS1) MANE Select	NP_067090.1:n.*595-7T>G
NM_001387438.1:c.326-7T>G (GDF1)	NP_001374367.1:n.326-7T>G
NM_001387440.1:c.*1180T>G (CERS1)	NP_001374369.1:n.*1180T>G