Canonical Allele Identifier: CA1830496436

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558651_6558652delinsTG , CM000671.2:g.6558651_6558652delinsTG	GRCh38
NC_000009.11:g.6558651_6558652delinsTG , CM000671.1:g.6558651_6558652delinsTG	GRCh37
NC_000009.10:g.6548651_6548652delinsTG	NCBI36
NG_016397.1:g.92041_92042delinsCA , LRG_643:g.92041_92042delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1959_1960delinsCA MANE Select	ENSP00000370737.4:p.Thr653=
ENST00000460457.2:n.119_120delinsCA
ENST00000638233.1:n.394_395delinsCA
ENST00000638661.1:c.159_160delinsCA	ENSP00000491369.1:p.Thr53=
ENST00000638694.1:n.146_147delinsCA
ENST00000639318.1:c.159_160delinsCA	ENSP00000491932.1:p.Thr53=
ENST00000639364.1:n.1659_1660delinsCA
ENST00000639443.1:n.1527_1528delinsCA
ENST00000639954.1:n.1667_1668delinsCA
ENST00000640208.1:c.159_160delinsCA	ENSP00000491895.1:p.Thr53=
ENST00000640505.1:n.198_199delinsCA
ENST00000640592.1:n.1842_1843delinsCA
ENST00000321612.6:c.1959_1960delinsCA	ENSP00000370737.3:p.Thr653=
ENST00000460457.1:n.98_99delinsCA
NM_000170.2:c.1959_1960delinsCA , LRG_643t1:c.1959_1960delinsCA	NP_000161.2:p.Thr653=
NM_000170.3:c.1959_1960delinsCA MANE Select	NP_000161.2:p.Thr653=