Canonical Allele Identifier: CA372881886

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558600C>A (hg19) ; chr9:g.6558600C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558600C>A , CM000671.2:g.6558600C>A	GRCh38
NC_000009.11:g.6558600C>A , CM000671.1:g.6558600C>A	GRCh37
NC_000009.10:g.6548600C>A	NCBI36
NG_016397.1:g.92093G>T , LRG_643:g.92093G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2011G>T MANE Select	ENSP00000370737.4:p.Asp671Tyr
ENST00000460457.2:n.171G>T
ENST00000638233.1:n.446G>T
ENST00000638661.1:c.211G>T	ENSP00000491369.1:p.Asp71Tyr
ENST00000638694.1:n.198G>T
ENST00000639318.1:c.211G>T	ENSP00000491932.1:p.Asp71Tyr
ENST00000639364.1:n.1711G>T
ENST00000639443.1:n.1579G>T
ENST00000639954.1:n.1719G>T
ENST00000640208.1:c.211G>T	ENSP00000491895.1:p.Asp71Tyr
ENST00000640505.1:n.250G>T
ENST00000640592.1:n.1894G>T
ENST00000321612.6:c.2011G>T	ENSP00000370737.3:p.Asp671Tyr
ENST00000460457.1:n.150G>T
NM_000170.2:c.2011G>T , LRG_643t1:c.2011G>T	NP_000161.2:p.Asp671Tyr
NM_000170.3:c.2011G>T MANE Select	NP_000161.2:p.Asp671Tyr