Canonical Allele Identifier: CA1830494082
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556617_6556618delinsAC , CM000671.2:g.6556617_6556618delinsAC GRCh38
NC_000009.11:g.6556617_6556618delinsAC , CM000671.1:g.6556617_6556618delinsAC GRCh37
NC_000009.10:g.6546617_6546618delinsAC NCBI36
NG_016397.1:g.94075_94076delinsGT , LRG_643:g.94075_94076delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2053-316_2053-315delinsGT MANE Select ENSP00000370737.4:n.2053-316_2053-315delinsGT
ENST00000638233.1:n.488-316_488-315delinsGT
ENST00000638661.1:c.253-316_253-315delinsGT ENSP00000491369.1:n.253-316_253-315delinsGT
ENST00000638694.1:n.240-316_240-315delinsGT
ENST00000639318.1:c.253-316_253-315delinsGT ENSP00000491932.1:n.253-316_253-315delinsGT
ENST00000639364.1:n.1753-316_1753-315delinsGT
ENST00000639443.1:n.1621-316_1621-315delinsGT
ENST00000639954.1:n.1761-316_1761-315delinsGT
ENST00000640505.1:n.292-316_292-315delinsGT
ENST00000321612.6:c.2053-316_2053-315delinsGT ENSP00000370737.3:n.2053-316_2053-315delinsGT
NM_000170.2:c.2053-316_2053-315delinsGT , LRG_643t1:c.2053-316_2053-315delinsGT NP_000161.2:n.2053-316_2053-315delinsGT
NM_000170.3:c.2053-316_2053-315delinsGT MANE Select NP_000161.2:n.2053-316_2053-315delinsGT