Canonical Allele Identifier: CA2689358831

Gene: GLDC

Linked Data

• gnomAD v4: 9-6558750-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558750A>G , CM000671.2:g.6558750A>G	GRCh38
NC_000009.11:g.6558750A>G , CM000671.1:g.6558750A>G	GRCh37
NC_000009.10:g.6548750A>G	NCBI36
NG_016397.1:g.91943T>C , LRG_643:g.91943T>C

Transcript Alleles

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