Canonical Allele Identifier: CA372882015

Gene: GLDC

Linked Data

• dbSNP Id: rs1311599421
• gnomAD v2: 9-6558645-C-T
• gnomAD v4: 9-6558645-C-T
• MyVariant Identifiers: chr9:g.6558645C>T (hg19) ; chr9:g.6558645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558645C>T , CM000671.2:g.6558645C>T	GRCh38
NC_000009.11:g.6558645C>T , CM000671.1:g.6558645C>T	GRCh37
NC_000009.10:g.6548645C>T	NCBI36
NG_016397.1:g.92048G>A , LRG_643:g.92048G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1966G>A MANE Select	ENSP00000370737.4:p.Ala656Thr
ENST00000460457.2:n.126G>A
ENST00000638233.1:n.401G>A
ENST00000638661.1:c.166G>A	ENSP00000491369.1:p.Ala56Thr
ENST00000638694.1:n.153G>A
ENST00000639318.1:c.166G>A	ENSP00000491932.1:p.Ala56Thr
ENST00000639364.1:n.1666G>A
ENST00000639443.1:n.1534G>A
ENST00000639954.1:n.1674G>A
ENST00000640208.1:c.166G>A	ENSP00000491895.1:p.Ala56Thr
ENST00000640505.1:n.205G>A
ENST00000640592.1:n.1849G>A
ENST00000321612.6:c.1966G>A	ENSP00000370737.3:p.Ala656Thr
ENST00000460457.1:n.105G>A
NM_000170.2:c.1966G>A , LRG_643t1:c.1966G>A	NP_000161.2:p.Ala656Thr
NM_000170.3:c.1966G>A MANE Select	NP_000161.2:p.Ala656Thr