Canonical Allele Identifier: CA1830496232
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558553A= , CM000671.2:g.6558553A= GRCh38
NC_000009.11:g.6558553A= , CM000671.1:g.6558553A= GRCh37
NC_000009.10:g.6548553A= NCBI36
NG_016397.1:g.92140T= , LRG_643:g.92140T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2052+6T= MANE Select ENSP00000370737.4:n.2052+6T=
ENST00000460457.2:n.212+6T=
ENST00000638233.1:n.487+6T=
ENST00000638661.1:c.252+6T= ENSP00000491369.1:n.252+6T=
ENST00000638694.1:n.239+6T=
ENST00000639318.1:c.252+6T= ENSP00000491932.1:n.252+6T=
ENST00000639364.1:n.1752+6T=
ENST00000639443.1:n.1620+6T=
ENST00000639954.1:n.1760+6T=
ENST00000640208.1:c.258T= ENSP00000491895.1:p.Leu86=
ENST00000640505.1:n.291+6T=
ENST00000640592.1:n.1941T=
ENST00000321612.6:c.2052+6T= ENSP00000370737.3:n.2052+6T=
ENST00000460457.1:n.197T=
NM_000170.2:c.2052+6T= , LRG_643t1:c.2052+6T= NP_000161.2:n.2052+6T=
NM_000170.3:c.2052+6T= MANE Select NP_000161.2:n.2052+6T=