Canonical Allele Identifier: CA1830493992

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556550_6556551delinsTG , CM000671.2:g.6556550_6556551delinsTG	GRCh38
NC_000009.11:g.6556550_6556551delinsTG , CM000671.1:g.6556550_6556551delinsTG	GRCh37
NC_000009.10:g.6546550_6546551delinsTG	NCBI36
NG_016397.1:g.94142_94143delinsCA , LRG_643:g.94142_94143delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2053-249_2053-248delinsCA MANE Select	ENSP00000370737.4:n.2053-249_2053-248delinsCA
ENST00000638233.1:n.488-249_488-248delinsCA
ENST00000638661.1:c.253-249_253-248delinsCA	ENSP00000491369.1:n.253-249_253-248delinsCA
ENST00000638694.1:n.240-249_240-248delinsCA
ENST00000639318.1:c.253-249_253-248delinsCA	ENSP00000491932.1:n.253-249_253-248delinsCA
ENST00000639364.1:n.1753-249_1753-248delinsCA
ENST00000639443.1:n.1621-249_1621-248delinsCA
ENST00000639954.1:n.1761-249_1761-248delinsCA
ENST00000640505.1:n.292-249_292-248delinsCA
ENST00000321612.6:c.2053-249_2053-248delinsCA	ENSP00000370737.3:n.2053-249_2053-248delinsCA
NM_000170.2:c.2053-249_2053-248delinsCA , LRG_643t1:c.2053-249_2053-248delinsCA	NP_000161.2:n.2053-249_2053-248delinsCA
NM_000170.3:c.2053-249_2053-248delinsCA MANE Select	NP_000161.2:n.2053-249_2053-248delinsCA