Canonical Allele Identifier: CA4980421

Gene: GLDC

Linked Data

• dbSNP Id: rs369827665
• ExAC: 9:6558532 C / T
• gnomAD v2: 9-6558532-C-T
• gnomAD v4: 9-6558532-C-T
• MyVariant Identifiers: chr9:g.6558532C>T (hg19) ; chr9:g.6558532C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558532C>T , CM000671.2:g.6558532C>T	GRCh38
NC_000009.11:g.6558532C>T , CM000671.1:g.6558532C>T	GRCh37
NC_000009.10:g.6548532C>T	NCBI36
NG_016397.1:g.92161G>A , LRG_643:g.92161G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2052+27G>A MANE Select	ENSP00000370737.4:n.2052+27G>A
ENST00000460457.2:n.212+27G>A
ENST00000638233.1:n.487+27G>A
ENST00000638661.1:c.252+27G>A	ENSP00000491369.1:n.252+27G>A
ENST00000638694.1:n.239+27G>A
ENST00000639318.1:c.252+27G>A	ENSP00000491932.1:n.252+27G>A
ENST00000639364.1:n.1752+27G>A
ENST00000639443.1:n.1620+27G>A
ENST00000639954.1:n.1760+27G>A
ENST00000640208.1:c.279G>A	ENSP00000491895.1:p.Gly93=
ENST00000640505.1:n.291+27G>A
ENST00000640592.1:n.1962G>A
ENST00000321612.6:c.2052+27G>A	ENSP00000370737.3:n.2052+27G>A
ENST00000460457.1:n.218G>A
NM_000170.2:c.2052+27G>A , LRG_643t1:c.2052+27G>A	NP_000161.2:n.2052+27G>A
NM_000170.3:c.2052+27G>A MANE Select	NP_000161.2:n.2052+27G>A