Canonical Allele Identifier: CA372881860

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558588T>C (hg19) ; chr9:g.6558588T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558588T>C , CM000671.2:g.6558588T>C	GRCh38
NC_000009.11:g.6558588T>C , CM000671.1:g.6558588T>C	GRCh37
NC_000009.10:g.6548588T>C	NCBI36
NG_016397.1:g.92105A>G , LRG_643:g.92105A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2023A>G MANE Select	ENSP00000370737.4:p.Asn675Asp
ENST00000460457.2:n.183A>G
ENST00000638233.1:n.458A>G
ENST00000638661.1:c.223A>G	ENSP00000491369.1:p.Asn75Asp
ENST00000638694.1:n.210A>G
ENST00000639318.1:c.223A>G	ENSP00000491932.1:p.Asn75Asp
ENST00000639364.1:n.1723A>G
ENST00000639443.1:n.1591A>G
ENST00000639954.1:n.1731A>G
ENST00000640208.1:c.223A>G	ENSP00000491895.1:p.Asn75Asp
ENST00000640505.1:n.262A>G
ENST00000640592.1:n.1906A>G
ENST00000321612.6:c.2023A>G	ENSP00000370737.3:p.Asn675Asp
ENST00000460457.1:n.162A>G
NM_000170.2:c.2023A>G , LRG_643t1:c.2023A>G	NP_000161.2:p.Asn675Asp
NM_000170.3:c.2023A>G MANE Select	NP_000161.2:p.Asn675Asp