Canonical Allele Identifier: CA865905281

Gene: GLDC

Linked Data

• dbSNP Id: rs1279794359
• gnomAD v4: 9-6558784-C-T
• MyVariant Identifiers: chr9:g.6558784C>T (hg19) ; chr9:g.6558784C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558784C>T , CM000671.2:g.6558784C>T	GRCh38
NC_000009.11:g.6558784C>T , CM000671.1:g.6558784C>T	GRCh37
NC_000009.10:g.6548784C>T	NCBI36
NG_016397.1:g.91909G>A , LRG_643:g.91909G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1927-100G>A MANE Select	ENSP00000370737.4:n.1927-100G>A
ENST00000460457.2:n.87-100G>A
ENST00000638233.1:n.362-100G>A
ENST00000638661.1:c.127-100G>A	ENSP00000491369.1:n.127-100G>A
ENST00000638694.1:n.114-100G>A
ENST00000639318.1:c.127-100G>A	ENSP00000491932.1:n.127-100G>A
ENST00000639364.1:n.1627-100G>A
ENST00000639443.1:n.1495-100G>A
ENST00000639954.1:n.1635-100G>A
ENST00000640208.1:c.127-100G>A	ENSP00000491895.1:n.127-100G>A
ENST00000640505.1:n.166-100G>A
ENST00000640592.1:n.1810-100G>A
ENST00000321612.6:c.1927-100G>A	ENSP00000370737.3:n.1927-100G>A
ENST00000460457.1:n.66-100G>A
NM_000170.2:c.1927-100G>A , LRG_643t1:c.1927-100G>A	NP_000161.2:n.1927-100G>A
NM_000170.3:c.1927-100G>A MANE Select	NP_000161.2:n.1927-100G>A