Canonical Allele Identifier: CA1830496379

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558612G= , CM000671.2:g.6558612G=	GRCh38
NC_000009.11:g.6558612G= , CM000671.1:g.6558612G=	GRCh37
NC_000009.10:g.6548612G=	NCBI36
NG_016397.1:g.92081C= , LRG_643:g.92081C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1999C= MANE Select	ENSP00000370737.4:p.Pro667=
ENST00000460457.2:n.159C=
ENST00000638233.1:n.434C=
ENST00000638661.1:c.199C=	ENSP00000491369.1:p.Pro67=
ENST00000638694.1:n.186C=
ENST00000639318.1:c.199C=	ENSP00000491932.1:p.Pro67=
ENST00000639364.1:n.1699C=
ENST00000639443.1:n.1567C=
ENST00000639954.1:n.1707C=
ENST00000640208.1:c.199C=	ENSP00000491895.1:p.Pro67=
ENST00000640505.1:n.238C=
ENST00000640592.1:n.1882C=
ENST00000321612.6:c.1999C=	ENSP00000370737.3:p.Pro667=
ENST00000460457.1:n.138C=
NM_000170.2:c.1999C= , LRG_643t1:c.1999C=	NP_000161.2:p.Pro667=
NM_000170.3:c.1999C= MANE Select	NP_000161.2:p.Pro667=