Canonical Allele Identifier: CA188652623

Gene: GLDC

Linked Data

• dbSNP Id: rs1003007981
• MyVariant Identifiers: chr9:g.6565267T>C (hg19) ; chr9:g.6565267T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6565267T>C , CM000671.2:g.6565267T>C	GRCh38
NC_000009.11:g.6565267T>C , CM000671.1:g.6565267T>C	GRCh37
NC_000009.10:g.6555267T>C	NCBI36
NG_016397.1:g.85426A>G , LRG_643:g.85426A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.1926+87A>G MANE Select	ENSP00000370737.4:n.1926+87A>G
ENST00000460457.2:n.86+87A>G
ENST00000638233.1:n.361+87A>G
ENST00000638661.1:c.126+87A>G	ENSP00000491369.1:n.126+87A>G
ENST00000638694.1:n.113+87A>G
ENST00000639318.1:c.126+87A>G	ENSP00000491932.1:n.126+87A>G
ENST00000639364.1:n.1626+87A>G
ENST00000639443.1:n.1494+87A>G
ENST00000639954.1:n.1634+87A>G
ENST00000640208.1:c.126+87A>G	ENSP00000491895.1:n.126+87A>G
ENST00000640505.1:n.165+87A>G
ENST00000640592.1:n.1809+87A>G
ENST00000321612.6:c.1926+87A>G	ENSP00000370737.3:n.1926+87A>G
ENST00000460457.1:n.65+87A>G
NM_000170.2:c.1926+87A>G , LRG_643t1:c.1926+87A>G	NP_000161.2:n.1926+87A>G
NM_000170.3:c.1926+87A>G MANE Select	NP_000161.2:n.1926+87A>G