Canonical Allele Identifier: CA1830492873

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6555844_6555845delinsCA , CM000671.2:g.6555844_6555845delinsCA	GRCh38
NC_000009.11:g.6555844_6555845delinsCA , CM000671.1:g.6555844_6555845delinsCA	GRCh37
NC_000009.10:g.6545844_6545845delinsCA	NCBI36
NG_016397.1:g.94848_94849delinsTG , LRG_643:g.94848_94849delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2202+308_2202+309delinsTG MANE Select	ENSP00000370737.4:n.2202+308_2202+309delinsTG
ENST00000638233.1:n.637+308_637+309delinsTG
ENST00000638661.1:c.402+308_402+309delinsTG	ENSP00000491369.1:n.402+308_402+309delinsTG
ENST00000638694.1:n.389+308_389+309delinsTG
ENST00000639318.1:c.402+308_402+309delinsTG	ENSP00000491932.1:n.402+308_402+309delinsTG
ENST00000639364.1:n.1902+308_1902+309delinsTG
ENST00000639443.1:n.1770+308_1770+309delinsTG
ENST00000639954.1:n.1910+308_1910+309delinsTG
ENST00000640505.1:n.441+308_441+309delinsTG
ENST00000321612.6:c.2202+308_2202+309delinsTG	ENSP00000370737.3:n.2202+308_2202+309delinsTG
NM_000170.2:c.2202+308_2202+309delinsTG , LRG_643t1:c.2202+308_2202+309delinsTG	NP_000161.2:n.2202+308_2202+309delinsTG
NM_000170.3:c.2202+308_2202+309delinsTG MANE Select	NP_000161.2:n.2202+308_2202+309delinsTG