Canonical Allele Identifier: CA372881940

Gene: GLDC

Linked Data

• gnomAD v4: 9-6558624-T-C
• MyVariant Identifiers: chr9:g.6558624T>C (hg19) ; chr9:g.6558624T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558624T>C , CM000671.2:g.6558624T>C	GRCh38
NC_000009.11:g.6558624T>C , CM000671.1:g.6558624T>C	GRCh37
NC_000009.10:g.6548624T>C	NCBI36
NG_016397.1:g.92069A>G , LRG_643:g.92069A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1987A>G MANE Select	ENSP00000370737.4:p.Met663Val
ENST00000460457.2:n.147A>G
ENST00000638233.1:n.422A>G
ENST00000638661.1:c.187A>G	ENSP00000491369.1:p.Met63Val
ENST00000638694.1:n.174A>G
ENST00000639318.1:c.187A>G	ENSP00000491932.1:p.Met63Val
ENST00000639364.1:n.1687A>G
ENST00000639443.1:n.1555A>G
ENST00000639954.1:n.1695A>G
ENST00000640208.1:c.187A>G	ENSP00000491895.1:p.Met63Val
ENST00000640505.1:n.226A>G
ENST00000640592.1:n.1870A>G
ENST00000321612.6:c.1987A>G	ENSP00000370737.3:p.Met663Val
ENST00000460457.1:n.126A>G
NM_000170.2:c.1987A>G , LRG_643t1:c.1987A>G	NP_000161.2:p.Met663Val
NM_000170.3:c.1987A>G MANE Select	NP_000161.2:p.Met663Val