Canonical Allele Identifier: CA1830496400

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558630C= , CM000671.2:g.6558630C=	GRCh38
NC_000009.11:g.6558630C= , CM000671.1:g.6558630C=	GRCh37
NC_000009.10:g.6548630C=	NCBI36
NG_016397.1:g.92063G= , LRG_643:g.92063G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1981G= MANE Select	ENSP00000370737.4:p.Ala661=
ENST00000460457.2:n.141G=
ENST00000638233.1:n.416G=
ENST00000638661.1:c.181G=	ENSP00000491369.1:p.Ala61=
ENST00000638694.1:n.168G=
ENST00000639318.1:c.181G=	ENSP00000491932.1:p.Ala61=
ENST00000639364.1:n.1681G=
ENST00000639443.1:n.1549G=
ENST00000639954.1:n.1689G=
ENST00000640208.1:c.181G=	ENSP00000491895.1:p.Ala61=
ENST00000640505.1:n.220G=
ENST00000640592.1:n.1864G=
ENST00000321612.6:c.1981G=	ENSP00000370737.3:p.Ala661=
ENST00000460457.1:n.120G=
NM_000170.2:c.1981G= , LRG_643t1:c.1981G=	NP_000161.2:p.Ala661=
NM_000170.3:c.1981G= MANE Select	NP_000161.2:p.Ala661=