Canonical Allele Identifier: CA586157452

Gene: GLDC

Linked Data

• dbSNP Id: rs1292293093
• gnomAD v2: 9-6556333-G-A
• gnomAD v3: 9-6556333-G-A
• gnomAD v4: 9-6556333-G-A
• MyVariant Identifiers: chr9:g.6556333G>A (hg19) ; chr9:g.6556333G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556333G>A , CM000671.2:g.6556333G>A	GRCh38
NC_000009.11:g.6556333G>A , CM000671.1:g.6556333G>A	GRCh37
NC_000009.10:g.6546333G>A	NCBI36
NG_016397.1:g.94360C>T , LRG_643:g.94360C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.2053-31C>T MANE Select	ENSP00000370737.4:n.2053-31C>T
ENST00000638233.1:n.488-31C>T
ENST00000638661.1:c.253-31C>T	ENSP00000491369.1:n.253-31C>T
ENST00000638694.1:n.240-31C>T
ENST00000639318.1:c.253-31C>T	ENSP00000491932.1:n.253-31C>T
ENST00000639364.1:n.1753-31C>T
ENST00000639443.1:n.1621-31C>T
ENST00000639954.1:n.1761-31C>T
ENST00000640505.1:n.292-31C>T
ENST00000321612.6:c.2053-31C>T	ENSP00000370737.3:n.2053-31C>T
NM_000170.2:c.2053-31C>T , LRG_643t1:c.2053-31C>T	NP_000161.2:n.2053-31C>T
NM_000170.3:c.2053-31C>T MANE Select	NP_000161.2:n.2053-31C>T