Canonical Allele Identifier: CA404862022

Gene: CERS1 GDF1

Linked Data

• dbSNP Id: rs1064793138
• gnomAD v3: 19-18868764-C-A
• gnomAD v4: 19-18868764-C-A
• MyVariant Identifiers: chr19:g.18979573C>A (hg19) ; chr19:g.18868764C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18868764C>A , CM000681.2:g.18868764C>A	GRCh38
NC_000019.9:g.18979573C>A , CM000681.1:g.18979573C>A	GRCh37
NC_000019.8:g.18840573C>A	NCBI36
NG_012070.1:g.32381G>T
NG_033056.1:g.32381G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000623882.4:c.*1221G>T (CERS1) MANE Select	ENSP00000485308.1:n.*1221G>T
ENST00000247005.8:c.952G>T (GDF1) MANE Select	ENSP00000247005.5:p.Ala318Ser
ENST00000247005.7:c.952G>T (GDF1)	ENSP00000247005.5:p.Ala318Ser
ENST00000623882.3:c.*1221G>T (CERS1)	ENSP00000485308.1:n.*1221G>T
ENST00000623927.1:c.952G>T (CERS1)	ENSP00000485582.1:p.Ala318Ser
NM_001492.5:c.952G>T (GDF1)	NP_001483.3:p.Ala318Ser
NM_021267.4:c.*1221G>T (CERS1)	NP_067090.1:n.*1221G>T
NM_001492.6:c.952G>T (GDF1) MANE Select	NP_001483.3:p.Ala318Ser
NM_021267.5:c.*1221G>T (CERS1) MANE Select	NP_067090.1:n.*1221G>T
NM_001387438.1:c.952G>T (GDF1)	NP_001374367.1:p.Ala318Ser
NM_001387440.1:c.*1813G>T (CERS1)	NP_001374369.1:n.*1813G>T