Canonical Allele Identifier: CA463585563

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556279T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556279T>C , CM000671.2:g.6556279T>C	GRCh38
NC_000009.11:g.6556279T>C , CM000671.1:g.6556279T>C	GRCh37
NC_000009.10:g.6546279T>C	NCBI36
NG_016397.1:g.94414A>G , LRG_643:g.94414A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2076A>G MANE Select	ENSP00000370737.4:p.Leu692=
ENST00000638233.1:n.511A>G
ENST00000638661.1:c.276A>G	ENSP00000491369.1:p.Leu92=
ENST00000638694.1:n.263A>G
ENST00000639318.1:c.276A>G	ENSP00000491932.1:p.Leu92=
ENST00000639364.1:n.1776A>G
ENST00000639443.1:n.1644A>G
ENST00000639954.1:n.1784A>G
ENST00000640505.1:n.315A>G
ENST00000321612.6:c.2076A>G	ENSP00000370737.3:p.Leu692=
NM_000170.2:c.2076A>G , LRG_643t1:c.2076A>G	NP_000161.2:p.Leu692=
NM_000170.3:c.2076A>G MANE Select	NP_000161.2:p.Leu692=