Canonical Allele Identifier: CA653151046

Gene: GLDC

Linked Data

• gnomAD v4: 9-6565276-G-T
• COSMIC: COSN26482257

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6565276G>T , CM000671.2:g.6565276G>T	GRCh38
NC_000009.11:g.6565276G>T , CM000671.1:g.6565276G>T	GRCh37
NC_000009.10:g.6555276G>T	NCBI36
NG_016397.1:g.85417C>A , LRG_643:g.85417C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.1926+78C>A MANE Select	ENSP00000370737.4:n.1926+78C>A
ENST00000460457.2:n.86+78C>A
ENST00000638233.1:n.361+78C>A
ENST00000638661.1:c.126+78C>A	ENSP00000491369.1:n.126+78C>A
ENST00000638694.1:n.113+78C>A
ENST00000639318.1:c.126+78C>A	ENSP00000491932.1:n.126+78C>A
ENST00000639364.1:n.1626+78C>A
ENST00000639443.1:n.1494+78C>A
ENST00000639954.1:n.1634+78C>A
ENST00000640208.1:c.126+78C>A	ENSP00000491895.1:n.126+78C>A
ENST00000640505.1:n.165+78C>A
ENST00000640592.1:n.1809+78C>A
ENST00000321612.6:c.1926+78C>A	ENSP00000370737.3:n.1926+78C>A
ENST00000460457.1:n.65+78C>A
NM_000170.2:c.1926+78C>A , LRG_643t1:c.1926+78C>A	NP_000161.2:n.1926+78C>A
NM_000170.3:c.1926+78C>A MANE Select	NP_000161.2:n.1926+78C>A