Canonical Allele Identifier: CA1830496189

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558532C= , CM000671.2:g.6558532C=	GRCh38
NC_000009.11:g.6558532C= , CM000671.1:g.6558532C=	GRCh37
NC_000009.10:g.6548532C=	NCBI36
NG_016397.1:g.92161G= , LRG_643:g.92161G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2052+27G= MANE Select	ENSP00000370737.4:n.2052+27G=
ENST00000460457.2:n.212+27G=
ENST00000638233.1:n.487+27G=
ENST00000638661.1:c.252+27G=	ENSP00000491369.1:n.252+27G=
ENST00000638694.1:n.239+27G=
ENST00000639318.1:c.252+27G=	ENSP00000491932.1:n.252+27G=
ENST00000639364.1:n.1752+27G=
ENST00000639443.1:n.1620+27G=
ENST00000639954.1:n.1760+27G=
ENST00000640208.1:c.279G=	ENSP00000491895.1:p.Gly93=
ENST00000640505.1:n.291+27G=
ENST00000640592.1:n.1962G=
ENST00000321612.6:c.2052+27G=	ENSP00000370737.3:n.2052+27G=
ENST00000460457.1:n.218G=
NM_000170.2:c.2052+27G= , LRG_643t1:c.2052+27G=	NP_000161.2:n.2052+27G=
NM_000170.3:c.2052+27G= MANE Select	NP_000161.2:n.2052+27G=