Canonical Allele Identifier: CA1830496669

Gene: GLDC

Linked Data

• dbSNP Id: rs1317022738

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558852C>T , CM000671.2:g.6558852C>T	GRCh38
NC_000009.11:g.6558852C>T , CM000671.1:g.6558852C>T	GRCh37
NC_000009.10:g.6548852C>T	NCBI36
NG_016397.1:g.91841G>A , LRG_643:g.91841G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1927-168G>A MANE Select	ENSP00000370737.4:n.1927-168G>A
ENST00000460457.2:n.87-168G>A
ENST00000638233.1:n.362-168G>A
ENST00000638661.1:c.127-168G>A	ENSP00000491369.1:n.127-168G>A
ENST00000638694.1:n.114-168G>A
ENST00000639318.1:c.127-168G>A	ENSP00000491932.1:n.127-168G>A
ENST00000639364.1:n.1627-168G>A
ENST00000639443.1:n.1495-168G>A
ENST00000639954.1:n.1635-168G>A
ENST00000640208.1:c.127-168G>A	ENSP00000491895.1:n.127-168G>A
ENST00000640505.1:n.166-168G>A
ENST00000640592.1:n.1810-168G>A
ENST00000321612.6:c.1927-168G>A	ENSP00000370737.3:n.1927-168G>A
ENST00000460457.1:n.66-168G>A
NM_000170.2:c.1927-168G>A , LRG_643t1:c.1927-168G>A	NP_000161.2:n.1927-168G>A
NM_000170.3:c.1927-168G>A MANE Select	NP_000161.2:n.1927-168G>A