Canonical Allele Identifier: CA372881829

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558571G>T (hg19) ; chr9:g.6558571G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558571G>T , CM000671.2:g.6558571G>T	GRCh38
NC_000009.11:g.6558571G>T , CM000671.1:g.6558571G>T	GRCh37
NC_000009.10:g.6548571G>T	NCBI36
NG_016397.1:g.92122C>A , LRG_643:g.92122C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2040C>A MANE Select	ENSP00000370737.4:p.His680Gln
ENST00000460457.2:n.200C>A
ENST00000638233.1:n.475C>A
ENST00000638661.1:c.240C>A	ENSP00000491369.1:p.His80Gln
ENST00000638694.1:n.227C>A
ENST00000639318.1:c.240C>A	ENSP00000491932.1:p.His80Gln
ENST00000639364.1:n.1740C>A
ENST00000639443.1:n.1608C>A
ENST00000639954.1:n.1748C>A
ENST00000640208.1:c.240C>A	ENSP00000491895.1:p.His80Gln
ENST00000640505.1:n.279C>A
ENST00000640592.1:n.1923C>A
ENST00000321612.6:c.2040C>A	ENSP00000370737.3:p.His680Gln
ENST00000460457.1:n.179C>A
NM_000170.2:c.2040C>A , LRG_643t1:c.2040C>A	NP_000161.2:p.His680Gln
NM_000170.3:c.2040C>A MANE Select	NP_000161.2:p.His680Gln