Canonical Allele Identifier: CA4980434

Gene: GLDC

Linked Data

• ClinVar Variation Id: 1383808
• ClinVar RCV Id: RCV001924681 ; RCV003222357 ; RCV002552877
• dbSNP Id: rs778376889
• ExAC: 9:6558576 C / T
• gnomAD v2: 9-6558576-C-T
• gnomAD v3: 9-6558576-C-T
• gnomAD v4: 9-6558576-C-T
• MyVariant Identifiers: chr9:g.6558576C>T (hg19) ; chr9:g.6558576C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558576C>T , CM000671.2:g.6558576C>T	GRCh38
NC_000009.11:g.6558576C>T , CM000671.1:g.6558576C>T	GRCh37
NC_000009.10:g.6548576C>T	NCBI36
NG_016397.1:g.92117G>A , LRG_643:g.92117G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2035G>A MANE Select	ENSP00000370737.4:p.Val679Ile
ENST00000460457.2:n.195G>A
ENST00000638233.1:n.470G>A
ENST00000638661.1:c.235G>A	ENSP00000491369.1:p.Val79Ile
ENST00000638694.1:n.222G>A
ENST00000639318.1:c.235G>A	ENSP00000491932.1:p.Val79Ile
ENST00000639364.1:n.1735G>A
ENST00000639443.1:n.1603G>A
ENST00000639954.1:n.1743G>A
ENST00000640208.1:c.235G>A	ENSP00000491895.1:p.Val79Ile
ENST00000640505.1:n.274G>A
ENST00000640592.1:n.1918G>A
ENST00000321612.6:c.2035G>A	ENSP00000370737.3:p.Val679Ile
ENST00000460457.1:n.174G>A
NM_000170.2:c.2035G>A , LRG_643t1:c.2035G>A	NP_000161.2:p.Val679Ile
NM_000170.3:c.2035G>A MANE Select	NP_000161.2:p.Val679Ile