Canonical Allele Identifier: CA4980029

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6534753G>A , CM000671.2:g.6534753G>A	GRCh38
NC_000009.11:g.6534753G>A , CM000671.1:g.6534753G>A	GRCh37
NC_000009.10:g.6524753G>A	NCBI36
NG_016397.1:g.115940C>T , LRG_643:g.115940C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000170.3:c.2874C>T MANE Select	NP_000161.2:p.Ser958=
ENST00000321612.8:c.2874C>T MANE Select	ENSP00000370737.4:p.Ser958=
NM_000170.2:c.2874C>T , LRG_643t1:c.2874C>T	NP_000161.2:p.Ser958=
ENST00000321612.6:c.2874C>T	ENSP00000370737.3:p.Ser958=
ENST00000477960.1:n.455C>T
ENST00000638233.1:n.1309C>T
ENST00000638274.1:c.26C>T
ENST00000638661.1:c.1074C>T	ENSP00000491369.1:p.Ser358=
ENST00000638694.1:n.1061C>T
ENST00000639318.1:c.978C>T	ENSP00000491932.1:p.Ser326=
ENST00000639364.1:n.2574C>T
ENST00000639443.1:n.2442C>T
ENST00000639461.1:n.1975C>T
ENST00000639639.1:c.576C>T	ENSP00000491312.1:p.Ser192=
ENST00000639954.1:n.2582C>T
ENST00000640505.1:n.1113C>T