Canonical Allele Identifier: CA4980449

Gene: GLDC

Linked Data

• ClinVar Variation Id: 2184309
• ClinVar RCV Id: RCV002632203
• dbSNP Id: rs753545868
• ExAC: 9:6558611 G / A
• gnomAD v2: 9-6558611-G-A
• gnomAD v4: 9-6558611-G-A
• MyVariant Identifiers: chr9:g.6558611G>A (hg19) ; chr9:g.6558611G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558611G>A , CM000671.2:g.6558611G>A	GRCh38
NC_000009.11:g.6558611G>A , CM000671.1:g.6558611G>A	GRCh37
NC_000009.10:g.6548611G>A	NCBI36
NG_016397.1:g.92082C>T , LRG_643:g.92082C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2000C>T MANE Select	ENSP00000370737.4:p.Pro667Leu
ENST00000460457.2:n.160C>T
ENST00000638233.1:n.435C>T
ENST00000638661.1:c.200C>T	ENSP00000491369.1:p.Pro67Leu
ENST00000638694.1:n.187C>T
ENST00000639318.1:c.200C>T	ENSP00000491932.1:p.Pro67Leu
ENST00000639364.1:n.1700C>T
ENST00000639443.1:n.1568C>T
ENST00000639954.1:n.1708C>T
ENST00000640208.1:c.200C>T	ENSP00000491895.1:p.Pro67Leu
ENST00000640505.1:n.239C>T
ENST00000640592.1:n.1883C>T
ENST00000321612.6:c.2000C>T	ENSP00000370737.3:p.Pro667Leu
ENST00000460457.1:n.139C>T
NM_000170.2:c.2000C>T , LRG_643t1:c.2000C>T	NP_000161.2:p.Pro667Leu
NM_000170.3:c.2000C>T MANE Select	NP_000161.2:p.Pro667Leu