Canonical Allele Identifier: CA372882249

Gene: GLDC

Linked Data

• ClinVar Variation Id: 1489319
• ClinVar RCV Id: RCV001980573
• dbSNP Id: rs2129735367
• MyVariant Identifiers: chr9:g.6558685C>T (hg19) ; chr9:g.6558685C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558685C>T , CM000671.2:g.6558685C>T	GRCh38
NC_000009.11:g.6558685C>T , CM000671.1:g.6558685C>T	GRCh37
NC_000009.10:g.6548685C>T	NCBI36
NG_016397.1:g.92008G>A , LRG_643:g.92008G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1927-1G>A MANE Select	ENSP00000370737.4:n.1927-1G>A
ENST00000460457.2:n.87-1G>A
ENST00000638233.1:n.362-1G>A
ENST00000638661.1:c.127-1G>A	ENSP00000491369.1:n.127-1G>A
ENST00000638694.1:n.114-1G>A
ENST00000639318.1:c.127-1G>A	ENSP00000491932.1:n.127-1G>A
ENST00000639364.1:n.1627-1G>A
ENST00000639443.1:n.1495-1G>A
ENST00000639954.1:n.1635-1G>A
ENST00000640208.1:c.127-1G>A	ENSP00000491895.1:n.127-1G>A
ENST00000640505.1:n.166-1G>A
ENST00000640592.1:n.1810-1G>A
ENST00000321612.6:c.1927-1G>A	ENSP00000370737.3:n.1927-1G>A
ENST00000460457.1:n.66-1G>A
NM_000170.2:c.1927-1G>A , LRG_643t1:c.1927-1G>A	NP_000161.2:n.1927-1G>A
NM_000170.3:c.1927-1G>A MANE Select	NP_000161.2:n.1927-1G>A