Canonical Allele Identifier: CA404862013

Gene: CERS1 GDF1

Linked Data

• MyVariant Identifiers: chr19:g.18979569A>C (hg19) ; chr19:g.18868760A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18868760A>C , CM000681.2:g.18868760A>C	GRCh38
NC_000019.9:g.18979569A>C , CM000681.1:g.18979569A>C	GRCh37
NC_000019.8:g.18840569A>C	NCBI36
NG_012070.1:g.32385T>G
NG_033056.1:g.32385T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623882.4:c.*1225T>G (CERS1) MANE Select	ENSP00000485308.1:n.*1225T>G
ENST00000247005.8:c.956T>G (GDF1) MANE Select	ENSP00000247005.5:p.Val319Gly
ENST00000247005.7:c.956T>G (GDF1)	ENSP00000247005.5:p.Val319Gly
ENST00000623882.3:c.*1225T>G (CERS1)	ENSP00000485308.1:n.*1225T>G
ENST00000623927.1:c.956T>G (CERS1)	ENSP00000485582.1:p.Val319Gly
NM_001492.5:c.956T>G (GDF1)	NP_001483.3:p.Val319Gly
NM_021267.4:c.*1225T>G (CERS1)	NP_067090.1:n.*1225T>G
NM_001492.6:c.956T>G (GDF1) MANE Select	NP_001483.3:p.Val319Gly
NM_021267.5:c.*1225T>G (CERS1) MANE Select	NP_067090.1:n.*1225T>G
NM_001387438.1:c.956T>G (GDF1)	NP_001374367.1:p.Val319Gly
NM_001387440.1:c.*1817T>G (CERS1)	NP_001374369.1:n.*1817T>G