Canonical Allele Identifier: CA1830496335
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558592A= , CM000671.2:g.6558592A= GRCh38
NC_000009.11:g.6558592A= , CM000671.1:g.6558592A= GRCh37
NC_000009.10:g.6548592A= NCBI36
NG_016397.1:g.92101T= , LRG_643:g.92101T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2019T= MANE Select ENSP00000370737.4:p.Tyr673=
ENST00000460457.2:n.179T=
ENST00000638233.1:n.454T=
ENST00000638661.1:c.219T= ENSP00000491369.1:p.Tyr73=
ENST00000638694.1:n.206T=
ENST00000639318.1:c.219T= ENSP00000491932.1:p.Tyr73=
ENST00000639364.1:n.1719T=
ENST00000639443.1:n.1587T=
ENST00000639954.1:n.1727T=
ENST00000640208.1:c.219T= ENSP00000491895.1:p.Tyr73=
ENST00000640505.1:n.258T=
ENST00000640592.1:n.1902T=
ENST00000321612.6:c.2019T= ENSP00000370737.3:p.Tyr673=
ENST00000460457.1:n.158T=
NM_000170.2:c.2019T= , LRG_643t1:c.2019T= NP_000161.2:p.Tyr673=
NM_000170.3:c.2019T= MANE Select NP_000161.2:p.Tyr673=