Canonical Allele Identifier: CA372881806

Gene: GLDC

Linked Data

• dbSNP Id: rs1452317734
• gnomAD v2: 9-6558561-T-C
• gnomAD v4: 9-6558561-T-C
• MyVariant Identifiers: chr9:g.6558561T>C (hg19) ; chr9:g.6558561T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558561T>C , CM000671.2:g.6558561T>C	GRCh38
NC_000009.11:g.6558561T>C , CM000671.1:g.6558561T>C	GRCh37
NC_000009.10:g.6548561T>C	NCBI36
NG_016397.1:g.92132A>G , LRG_643:g.92132A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2050A>G MANE Select	ENSP00000370737.4:p.Met684Val
ENST00000460457.2:n.210A>G
ENST00000638233.1:n.485A>G
ENST00000638661.1:c.250A>G	ENSP00000491369.1:p.Met84Val
ENST00000638694.1:n.237A>G
ENST00000639318.1:c.250A>G	ENSP00000491932.1:p.Met84Val
ENST00000639364.1:n.1750A>G
ENST00000639443.1:n.1618A>G
ENST00000639954.1:n.1758A>G
ENST00000640208.1:c.250A>G	ENSP00000491895.1:p.Met84Val
ENST00000640505.1:n.289A>G
ENST00000640592.1:n.1933A>G
ENST00000321612.6:c.2050A>G	ENSP00000370737.3:p.Met684Val
ENST00000460457.1:n.189A>G
NM_000170.2:c.2050A>G , LRG_643t1:c.2050A>G	NP_000161.2:p.Met684Val
NM_000170.3:c.2050A>G MANE Select	NP_000161.2:p.Met684Val