Canonical Allele Identifier: CA865905314

Gene: GLDC

Linked Data

• dbSNP Id: rs1440254250
• gnomAD v4: 9-6558832-A-C
• MyVariant Identifiers: chr9:g.6558832A>C (hg19) ; chr9:g.6558832A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558832A>C , CM000671.2:g.6558832A>C	GRCh38
NC_000009.11:g.6558832A>C , CM000671.1:g.6558832A>C	GRCh37
NC_000009.10:g.6548832A>C	NCBI36
NG_016397.1:g.91861T>G , LRG_643:g.91861T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1927-148T>G MANE Select	ENSP00000370737.4:n.1927-148T>G
ENST00000460457.2:n.87-148T>G
ENST00000638233.1:n.362-148T>G
ENST00000638661.1:c.127-148T>G	ENSP00000491369.1:n.127-148T>G
ENST00000638694.1:n.114-148T>G
ENST00000639318.1:c.127-148T>G	ENSP00000491932.1:n.127-148T>G
ENST00000639364.1:n.1627-148T>G
ENST00000639443.1:n.1495-148T>G
ENST00000639954.1:n.1635-148T>G
ENST00000640208.1:c.127-148T>G	ENSP00000491895.1:n.127-148T>G
ENST00000640505.1:n.166-148T>G
ENST00000640592.1:n.1810-148T>G
ENST00000321612.6:c.1927-148T>G	ENSP00000370737.3:n.1927-148T>G
ENST00000460457.1:n.66-148T>G
NM_000170.2:c.1927-148T>G , LRG_643t1:c.1927-148T>G	NP_000161.2:n.1927-148T>G
NM_000170.3:c.1927-148T>G MANE Select	NP_000161.2:n.1927-148T>G