Canonical Allele Identifier: CA372881170

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556160T>C (hg19) ; chr9:g.6556160T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556160T>C , CM000671.2:g.6556160T>C	GRCh38
NC_000009.11:g.6556160T>C , CM000671.1:g.6556160T>C	GRCh37
NC_000009.10:g.6546160T>C	NCBI36
NG_016397.1:g.94533A>G , LRG_643:g.94533A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2195A>G MANE Select	ENSP00000370737.4:p.Asn732Ser
ENST00000638233.1:n.630A>G
ENST00000638661.1:c.395A>G	ENSP00000491369.1:p.Asn132Ser
ENST00000638694.1:n.382A>G
ENST00000639318.1:c.395A>G	ENSP00000491932.1:p.Asn132Ser
ENST00000639364.1:n.1895A>G
ENST00000639443.1:n.1763A>G
ENST00000639954.1:n.1903A>G
ENST00000640505.1:n.434A>G
ENST00000321612.6:c.2195A>G	ENSP00000370737.3:p.Asn732Ser
NM_000170.2:c.2195A>G , LRG_643t1:c.2195A>G	NP_000161.2:p.Asn732Ser
NM_000170.3:c.2195A>G MANE Select	NP_000161.2:p.Asn732Ser