Canonical Allele Identifier: CA1830492810
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6555790_6555791delinsTA , CM000671.2:g.6555790_6555791delinsTA GRCh38
NC_000009.11:g.6555790_6555791delinsTA , CM000671.1:g.6555790_6555791delinsTA GRCh37
NC_000009.10:g.6545790_6545791delinsTA NCBI36
NG_016397.1:g.94902_94903delinsTA , LRG_643:g.94902_94903delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2202+362_2202+363delinsTA MANE Select ENSP00000370737.4:n.2202+362_2202+363delinsTA
ENST00000638233.1:n.637+362_637+363delinsTA
ENST00000638661.1:c.402+362_402+363delinsTA ENSP00000491369.1:n.402+362_402+363delinsTA
ENST00000638694.1:n.389+362_389+363delinsTA
ENST00000639318.1:c.402+362_402+363delinsTA ENSP00000491932.1:n.402+362_402+363delinsTA
ENST00000639364.1:n.1902+362_1902+363delinsTA
ENST00000639443.1:n.1770+362_1770+363delinsTA
ENST00000639954.1:n.1910+362_1910+363delinsTA
ENST00000640505.1:n.441+362_441+363delinsTA
ENST00000321612.6:c.2202+362_2202+363delinsTA ENSP00000370737.3:n.2202+362_2202+363delinsTA
NM_000170.2:c.2202+362_2202+363delinsTA , LRG_643t1:c.2202+362_2202+363delinsTA NP_000161.2:n.2202+362_2202+363delinsTA
NM_000170.3:c.2202+362_2202+363delinsTA MANE Select NP_000161.2:n.2202+362_2202+363delinsTA