Canonical Allele Identifier: CA372894402

Gene: GLDC

Linked Data

• gnomAD v4: 9-6595112-A-G
• MyVariant Identifiers: chr9:g.6595112A>G (hg19) ; chr9:g.6595112A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6595112A>G , CM000671.2:g.6595112A>G	GRCh38
NC_000009.11:g.6595112A>G , CM000671.1:g.6595112A>G	GRCh37
NC_000009.10:g.6585112A>G	NCBI36
NG_016397.1:g.55581T>C , LRG_643:g.55581T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.1163T>C MANE Select	ENSP00000370737.4:p.Leu388Ser
ENST00000638654.1:c.410T>C	ENSP00000491101.1:p.Leu137Ser
ENST00000639364.1:n.863T>C
ENST00000639443.1:n.731T>C
ENST00000639493.1:n.315T>C
ENST00000639954.1:n.871T>C
ENST00000640592.1:n.1046T>C
ENST00000321612.6:c.1163T>C	ENSP00000370737.3:p.Leu388Ser
ENST00000463305.1:n.247T>C
NM_000170.2:c.1163T>C , LRG_643t1:c.1163T>C	NP_000161.2:p.Leu388Ser
NM_000170.3:c.1163T>C MANE Select	NP_000161.2:p.Leu388Ser