Canonical Allele Identifier: CA1830496395

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558625G= , CM000671.2:g.6558625G=	GRCh38
NC_000009.11:g.6558625G= , CM000671.1:g.6558625G=	GRCh37
NC_000009.10:g.6548625G=	NCBI36
NG_016397.1:g.92068C= , LRG_643:g.92068C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1986C= MANE Select	ENSP00000370737.4:p.Gly662=
ENST00000460457.2:n.146C=
ENST00000638233.1:n.421C=
ENST00000638661.1:c.186C=	ENSP00000491369.1:p.Gly62=
ENST00000638694.1:n.173C=
ENST00000639318.1:c.186C=	ENSP00000491932.1:p.Gly62=
ENST00000639364.1:n.1686C=
ENST00000639443.1:n.1554C=
ENST00000639954.1:n.1694C=
ENST00000640208.1:c.186C=	ENSP00000491895.1:p.Gly62=
ENST00000640505.1:n.225C=
ENST00000640592.1:n.1869C=
ENST00000321612.6:c.1986C=	ENSP00000370737.3:p.Gly662=
ENST00000460457.1:n.125C=
NM_000170.2:c.1986C= , LRG_643t1:c.1986C=	NP_000161.2:p.Gly662=
NM_000170.3:c.1986C= MANE Select	NP_000161.2:p.Gly662=