Canonical Allele Identifier: CA2689358910

Gene: GLDC

Linked Data

• gnomAD v4: 9-6565253-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6565253G>A , CM000671.2:g.6565253G>A	GRCh38
NC_000009.11:g.6565253G>A , CM000671.1:g.6565253G>A	GRCh37
NC_000009.10:g.6555253G>A	NCBI36
NG_016397.1:g.85440C>T , LRG_643:g.85440C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.1926+101C>T MANE Select	ENSP00000370737.4:n.1926+101C>T
ENST00000460457.2:n.86+101C>T
ENST00000638233.1:n.361+101C>T
ENST00000638661.1:c.126+101C>T	ENSP00000491369.1:n.126+101C>T
ENST00000638694.1:n.113+101C>T
ENST00000639318.1:c.126+101C>T	ENSP00000491932.1:n.126+101C>T
ENST00000639364.1:n.1626+101C>T
ENST00000639443.1:n.1494+101C>T
ENST00000639954.1:n.1634+101C>T
ENST00000640208.1:c.126+101C>T	ENSP00000491895.1:n.126+101C>T
ENST00000640505.1:n.165+101C>T
ENST00000640592.1:n.1809+101C>T
ENST00000321612.6:c.1926+101C>T	ENSP00000370737.3:n.1926+101C>T
ENST00000460457.1:n.65+101C>T
NM_000170.2:c.1926+101C>T , LRG_643t1:c.1926+101C>T	NP_000161.2:n.1926+101C>T
NM_000170.3:c.1926+101C>T MANE Select	NP_000161.2:n.1926+101C>T