Canonical Allele Identifier: CA1830496443

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558654T= , CM000671.2:g.6558654T=	GRCh38
NC_000009.11:g.6558654T= , CM000671.1:g.6558654T=	GRCh37
NC_000009.10:g.6548654T=	NCBI36
NG_016397.1:g.92039A= , LRG_643:g.92039A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1957A= MANE Select	ENSP00000370737.4:p.Thr653=
ENST00000460457.2:n.117A=
ENST00000638233.1:n.392A=
ENST00000638661.1:c.157A=	ENSP00000491369.1:p.Thr53=
ENST00000638694.1:n.144A=
ENST00000639318.1:c.157A=	ENSP00000491932.1:p.Thr53=
ENST00000639364.1:n.1657A=
ENST00000639443.1:n.1525A=
ENST00000639954.1:n.1665A=
ENST00000640208.1:c.157A=	ENSP00000491895.1:p.Thr53=
ENST00000640505.1:n.196A=
ENST00000640592.1:n.1840A=
ENST00000321612.6:c.1957A=	ENSP00000370737.3:p.Thr653=
ENST00000460457.1:n.96A=
NM_000170.2:c.1957A= , LRG_643t1:c.1957A=	NP_000161.2:p.Thr653=
NM_000170.3:c.1957A= MANE Select	NP_000161.2:p.Thr653=