Canonical Allele Identifier: CA1830493858

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556431_6556435delinsCAAAG , CM000671.2:g.6556431_6556435delinsCAAAG	GRCh38
NC_000009.11:g.6556431_6556435delinsCAAAG , CM000671.1:g.6556431_6556435delinsCAAAG	GRCh37
NC_000009.10:g.6546431_6546435delinsCAAAG	NCBI36
NG_016397.1:g.94258_94262delinsCTTTG , LRG_643:g.94258_94262delinsCTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2053-133_2053-129delinsCTTTG MANE Select	ENSP00000370737.4:n.2053-133_2053-129delinsCTTTG
ENST00000638233.1:n.488-133_488-129delinsCTTTG
ENST00000638661.1:c.253-133_253-129delinsCTTTG	ENSP00000491369.1:n.253-133_253-129delinsCTTTG
ENST00000638694.1:n.240-133_240-129delinsCTTTG
ENST00000639318.1:c.253-133_253-129delinsCTTTG	ENSP00000491932.1:n.253-133_253-129delinsCTTTG
ENST00000639364.1:n.1753-133_1753-129delinsCTTTG
ENST00000639443.1:n.1621-133_1621-129delinsCTTTG
ENST00000639954.1:n.1761-133_1761-129delinsCTTTG
ENST00000640505.1:n.292-133_292-129delinsCTTTG
ENST00000321612.6:c.2053-133_2053-129delinsCTTTG	ENSP00000370737.3:n.2053-133_2053-129delinsCTTTG
NM_000170.2:c.2053-133_2053-129delinsCTTTG , LRG_643t1:c.2053-133_2053-129delinsCTTTG	NP_000161.2:n.2053-133_2053-129delinsCTTTG
NM_000170.3:c.2053-133_2053-129delinsCTTTG MANE Select	NP_000161.2:n.2053-133_2053-129delinsCTTTG