Canonical Allele Identifier: CA1830503814

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6565363C= , CM000671.2:g.6565363C=	GRCh38
NC_000009.11:g.6565363C= , CM000671.1:g.6565363C=	GRCh37
NC_000009.10:g.6555363C=	NCBI36
NG_016397.1:g.85330G= , LRG_643:g.85330G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.1917G= MANE Select	ENSP00000370737.4:p.Gly639=
ENST00000460457.2:n.77G=
ENST00000638233.1:n.352G=
ENST00000638661.1:c.117G=	ENSP00000491369.1:p.Gly39=
ENST00000638694.1:n.104G=
ENST00000639318.1:c.117G=	ENSP00000491932.1:p.Gly39=
ENST00000639364.1:n.1617G=
ENST00000639443.1:n.1485G=
ENST00000639954.1:n.1625G=
ENST00000640208.1:c.117G=	ENSP00000491895.1:p.Gly39=
ENST00000640505.1:n.156G=
ENST00000640592.1:n.1800G=
ENST00000321612.6:c.1917G=	ENSP00000370737.3:p.Gly639=
ENST00000460457.1:n.56G=
NM_000170.2:c.1917G= , LRG_643t1:c.1917G=	NP_000161.2:p.Gly639=
NM_000170.3:c.1917G= MANE Select	NP_000161.2:p.Gly639=