Canonical Allele Identifier: CA2782786473
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558804T>C , CM000671.2:g.6558804T>C GRCh38
NC_000009.11:g.6558804T>C , CM000671.1:g.6558804T>C GRCh37
NC_000009.10:g.6548804T>C NCBI36
NG_016397.1:g.91889A>G , LRG_643:g.91889A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1927-120A>G MANE Select ENSP00000370737.4:n.1927-120A>G
ENST00000460457.2:n.87-120A>G
ENST00000638233.1:n.362-120A>G
ENST00000638661.1:c.127-120A>G ENSP00000491369.1:n.127-120A>G
ENST00000638694.1:n.114-120A>G
ENST00000639318.1:c.127-120A>G ENSP00000491932.1:n.127-120A>G
ENST00000639364.1:n.1627-120A>G
ENST00000639443.1:n.1495-120A>G
ENST00000639954.1:n.1635-120A>G
ENST00000640208.1:c.127-120A>G ENSP00000491895.1:n.127-120A>G
ENST00000640505.1:n.166-120A>G
ENST00000640592.1:n.1810-120A>G
ENST00000321612.6:c.1927-120A>G ENSP00000370737.3:n.1927-120A>G
ENST00000460457.1:n.66-120A>G
NM_000170.2:c.1927-120A>G , LRG_643t1:c.1927-120A>G NP_000161.2:n.1927-120A>G
NM_000170.3:c.1927-120A>G MANE Select NP_000161.2:n.1927-120A>G