Canonical Allele Identifier: CA1830493743

Gene: GLDC

Linked Data

• dbSNP Id: rs1817631005

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556344_6556345del , CM000671.2:g.6556344_6556345del	GRCh38
NC_000009.11:g.6556344_6556345del , CM000671.1:g.6556344_6556345del	GRCh37
NC_000009.10:g.6546344_6546345del	NCBI36
NG_016397.1:g.94350_94351del , LRG_643:g.94350_94351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2053-41_2053-40del MANE Select	ENSP00000370737.4:n.2053-41_2053-40del
ENST00000638233.1:n.488-41_488-40del
ENST00000638661.1:c.253-41_253-40del	ENSP00000491369.1:n.253-41_253-40del
ENST00000638694.1:n.240-41_240-40del
ENST00000639318.1:c.253-41_253-40del	ENSP00000491932.1:n.253-41_253-40del
ENST00000639364.1:n.1753-41_1753-40del
ENST00000639443.1:n.1621-41_1621-40del
ENST00000639954.1:n.1761-41_1761-40del
ENST00000640505.1:n.292-41_292-40del
ENST00000321612.6:c.2053-41_2053-40del	ENSP00000370737.3:n.2053-41_2053-40del
NM_000170.2:c.2053-41_2053-40del , LRG_643t1:c.2053-41_2053-40del	NP_000161.2:n.2053-41_2053-40del
NM_000170.3:c.2053-41_2053-40del MANE Select	NP_000161.2:n.2053-41_2053-40del