Canonical Allele Identifier: CA1830496391

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558619C= , CM000671.2:g.6558619C=	GRCh38
NC_000009.11:g.6558619C= , CM000671.1:g.6558619C=	GRCh37
NC_000009.10:g.6548619C=	NCBI36
NG_016397.1:g.92074G= , LRG_643:g.92074G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1992G= MANE Select	ENSP00000370737.4:p.Lys664=
ENST00000460457.2:n.152G=
ENST00000638233.1:n.427G=
ENST00000638661.1:c.192G=	ENSP00000491369.1:p.Lys64=
ENST00000638694.1:n.179G=
ENST00000639318.1:c.192G=	ENSP00000491932.1:p.Lys64=
ENST00000639364.1:n.1692G=
ENST00000639443.1:n.1560G=
ENST00000639954.1:n.1700G=
ENST00000640208.1:c.192G=	ENSP00000491895.1:p.Lys64=
ENST00000640505.1:n.231G=
ENST00000640592.1:n.1875G=
ENST00000321612.6:c.1992G=	ENSP00000370737.3:p.Lys664=
ENST00000460457.1:n.131G=
NM_000170.2:c.1992G= , LRG_643t1:c.1992G=	NP_000161.2:p.Lys664=
NM_000170.3:c.1992G= MANE Select	NP_000161.2:p.Lys664=