Canonical Allele Identifier: CA506118668

Gene: CERS1 GDF1

Linked Data

• gnomAD v4: 19-18869206-C-T
• MyVariant Identifiers: chr19:g.18980015C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18869206C>T , CM000681.2:g.18869206C>T	GRCh38
NC_000019.9:g.18980015C>T , CM000681.1:g.18980015C>T	GRCh37
NC_000019.8:g.18841015C>T	NCBI36
NG_012070.1:g.31939G>A
NG_033056.1:g.31939G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623882.4:c.*779G>A (CERS1) MANE Select	ENSP00000485308.1:n.*779G>A
ENST00000247005.8:c.510G>A (GDF1) MANE Select	ENSP00000247005.5:p.Ala170=
ENST00000247005.7:c.510G>A (GDF1)	ENSP00000247005.5:p.Ala170=
ENST00000623882.3:c.*779G>A (CERS1)	ENSP00000485308.1:n.*779G>A
ENST00000623927.1:c.510G>A (CERS1)	ENSP00000485582.1:p.Ala170=
NM_001492.5:c.510G>A (GDF1)	NP_001483.3:p.Ala170=
NM_021267.4:c.*779G>A (CERS1)	NP_067090.1:n.*779G>A
NM_001492.6:c.510G>A (GDF1) MANE Select	NP_001483.3:p.Ala170=
NM_021267.5:c.*779G>A (CERS1) MANE Select	NP_067090.1:n.*779G>A
NM_001387438.1:c.510G>A (GDF1)	NP_001374367.1:p.Ala170=
NM_001387440.1:c.*1371G>A (CERS1)	NP_001374369.1:n.*1371G>A