Canonical Allele Identifier: CA1830496299

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558581T= , CM000671.2:g.6558581T=	GRCh38
NC_000009.11:g.6558581T= , CM000671.1:g.6558581T=	GRCh37
NC_000009.10:g.6548581T=	NCBI36
NG_016397.1:g.92112A= , LRG_643:g.92112A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2030A= MANE Select	ENSP00000370737.4:p.Asp677=
ENST00000460457.2:n.190A=
ENST00000638233.1:n.465A=
ENST00000638661.1:c.230A=	ENSP00000491369.1:p.Asp77=
ENST00000638694.1:n.217A=
ENST00000639318.1:c.230A=	ENSP00000491932.1:p.Asp77=
ENST00000639364.1:n.1730A=
ENST00000639443.1:n.1598A=
ENST00000639954.1:n.1738A=
ENST00000640208.1:c.230A=	ENSP00000491895.1:p.Asp77=
ENST00000640505.1:n.269A=
ENST00000640592.1:n.1913A=
ENST00000321612.6:c.2030A=	ENSP00000370737.3:p.Asp677=
ENST00000460457.1:n.169A=
NM_000170.2:c.2030A= , LRG_643t1:c.2030A=	NP_000161.2:p.Asp677=
NM_000170.3:c.2030A= MANE Select	NP_000161.2:p.Asp677=