Canonical Allele Identifier: CA463586998

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6565354C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6565354C>A , CM000671.2:g.6565354C>A	GRCh38
NC_000009.11:g.6565354C>A , CM000671.1:g.6565354C>A	GRCh37
NC_000009.10:g.6555354C>A	NCBI36
NG_016397.1:g.85339G>T , LRG_643:g.85339G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.1926G>T MANE Select	ENSP00000370737.4:p.Thr642=
ENST00000460457.2:n.86G>T
ENST00000638233.1:n.361G>T
ENST00000638661.1:c.126G>T	ENSP00000491369.1:p.Thr42=
ENST00000638694.1:n.113G>T
ENST00000639318.1:c.126G>T	ENSP00000491932.1:p.Thr42=
ENST00000639364.1:n.1626G>T
ENST00000639443.1:n.1494G>T
ENST00000639954.1:n.1634G>T
ENST00000640208.1:c.126G>T	ENSP00000491895.1:p.Thr42=
ENST00000640505.1:n.165G>T
ENST00000640592.1:n.1809G>T
ENST00000321612.6:c.1926G>T	ENSP00000370737.3:p.Thr642=
ENST00000460457.1:n.65G>T
NM_000170.2:c.1926G>T , LRG_643t1:c.1926G>T	NP_000161.2:p.Thr642=
NM_000170.3:c.1926G>T MANE Select	NP_000161.2:p.Thr642=