Canonical Allele Identifier: CA463585600

Gene: GLDC

Linked Data

• COSMIC: COSM4935016
• MyVariant Identifiers: chr9:g.6558589C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558589C>A , CM000671.2:g.6558589C>A	GRCh38
NC_000009.11:g.6558589C>A , CM000671.1:g.6558589C>A	GRCh37
NC_000009.10:g.6548589C>A	NCBI36
NG_016397.1:g.92104G>T , LRG_643:g.92104G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2022G>T MANE Select	ENSP00000370737.4:p.Gly674=
ENST00000460457.2:n.182G>T
ENST00000638233.1:n.457G>T
ENST00000638661.1:c.222G>T	ENSP00000491369.1:p.Gly74=
ENST00000638694.1:n.209G>T
ENST00000639318.1:c.222G>T	ENSP00000491932.1:p.Gly74=
ENST00000639364.1:n.1722G>T
ENST00000639443.1:n.1590G>T
ENST00000639954.1:n.1730G>T
ENST00000640208.1:c.222G>T	ENSP00000491895.1:p.Gly74=
ENST00000640505.1:n.261G>T
ENST00000640592.1:n.1905G>T
ENST00000321612.6:c.2022G>T	ENSP00000370737.3:p.Gly674=
ENST00000460457.1:n.161G>T
NM_000170.2:c.2022G>T , LRG_643t1:c.2022G>T	NP_000161.2:p.Gly674=
NM_000170.3:c.2022G>T MANE Select	NP_000161.2:p.Gly674=