Canonical Allele Identifier: CA1830492901

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6555862C= , CM000671.2:g.6555862C=	GRCh38
NC_000009.11:g.6555862C= , CM000671.1:g.6555862C=	GRCh37
NC_000009.10:g.6545862C=	NCBI36
NG_016397.1:g.94831G= , LRG_643:g.94831G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2202+291G= MANE Select	ENSP00000370737.4:n.2202+291G=
ENST00000638233.1:n.637+291G=
ENST00000638661.1:c.402+291G=	ENSP00000491369.1:n.402+291G=
ENST00000638694.1:n.389+291G=
ENST00000639318.1:c.402+291G=	ENSP00000491932.1:n.402+291G=
ENST00000639364.1:n.1902+291G=
ENST00000639443.1:n.1770+291G=
ENST00000639954.1:n.1910+291G=
ENST00000640505.1:n.441+291G=
ENST00000321612.6:c.2202+291G=	ENSP00000370737.3:n.2202+291G=
NM_000170.2:c.2202+291G= , LRG_643t1:c.2202+291G=	NP_000161.2:n.2202+291G=
NM_000170.3:c.2202+291G= MANE Select	NP_000161.2:n.2202+291G=