Canonical Allele Identifier: CA463585701

Gene: GLDC

Linked Data

• dbSNP Id: rs1817684418
• MyVariant Identifiers: chr9:g.6558619C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558619C>T , CM000671.2:g.6558619C>T	GRCh38
NC_000009.11:g.6558619C>T , CM000671.1:g.6558619C>T	GRCh37
NC_000009.10:g.6548619C>T	NCBI36
NG_016397.1:g.92074G>A , LRG_643:g.92074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1992G>A MANE Select	ENSP00000370737.4:p.Lys664=
ENST00000460457.2:n.152G>A
ENST00000638233.1:n.427G>A
ENST00000638661.1:c.192G>A	ENSP00000491369.1:p.Lys64=
ENST00000638694.1:n.179G>A
ENST00000639318.1:c.192G>A	ENSP00000491932.1:p.Lys64=
ENST00000639364.1:n.1692G>A
ENST00000639443.1:n.1560G>A
ENST00000639954.1:n.1700G>A
ENST00000640208.1:c.192G>A	ENSP00000491895.1:p.Lys64=
ENST00000640505.1:n.231G>A
ENST00000640592.1:n.1875G>A
ENST00000321612.6:c.1992G>A	ENSP00000370737.3:p.Lys664=
ENST00000460457.1:n.131G>A
NM_000170.2:c.1992G>A , LRG_643t1:c.1992G>A	NP_000161.2:p.Lys664=
NM_000170.3:c.1992G>A MANE Select	NP_000161.2:p.Lys664=