Canonical Allele Identifier: CA1830496186

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558530C= , CM000671.2:g.6558530C=	GRCh38
NC_000009.11:g.6558530C= , CM000671.1:g.6558530C=	GRCh37
NC_000009.10:g.6548530C=	NCBI36
NG_016397.1:g.92163G= , LRG_643:g.92163G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2052+29G= MANE Select	ENSP00000370737.4:n.2052+29G=
ENST00000460457.2:n.212+29G=
ENST00000638233.1:n.487+29G=
ENST00000638661.1:c.252+29G=	ENSP00000491369.1:n.252+29G=
ENST00000638694.1:n.239+29G=
ENST00000639318.1:c.252+29G=	ENSP00000491932.1:n.252+29G=
ENST00000639364.1:n.1752+29G=
ENST00000639443.1:n.1620+29G=
ENST00000639954.1:n.1760+29G=
ENST00000640208.1:c.281G=	ENSP00000491895.1:p.Arg94=
ENST00000640505.1:n.291+29G=
ENST00000640592.1:n.1964G=
ENST00000321612.6:c.2052+29G=	ENSP00000370737.3:n.2052+29G=
ENST00000460457.1:n.220G=
NM_000170.2:c.2052+29G= , LRG_643t1:c.2052+29G=	NP_000161.2:n.2052+29G=
NM_000170.3:c.2052+29G= MANE Select	NP_000161.2:n.2052+29G=