Canonical Allele Identifier: CA1830496377
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558610A= , CM000671.2:g.6558610A= GRCh38
NC_000009.11:g.6558610A= , CM000671.1:g.6558610A= GRCh37
NC_000009.10:g.6548610A= NCBI36
NG_016397.1:g.92083T= , LRG_643:g.92083T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2001T= MANE Select ENSP00000370737.4:p.Pro667=
ENST00000460457.2:n.161T=
ENST00000638233.1:n.436T=
ENST00000638661.1:c.201T= ENSP00000491369.1:p.Pro67=
ENST00000638694.1:n.188T=
ENST00000639318.1:c.201T= ENSP00000491932.1:p.Pro67=
ENST00000639364.1:n.1701T=
ENST00000639443.1:n.1569T=
ENST00000639954.1:n.1709T=
ENST00000640208.1:c.201T= ENSP00000491895.1:p.Pro67=
ENST00000640505.1:n.240T=
ENST00000640592.1:n.1884T=
ENST00000321612.6:c.2001T= ENSP00000370737.3:p.Pro667=
ENST00000460457.1:n.140T=
NM_000170.2:c.2001T= , LRG_643t1:c.2001T= NP_000161.2:p.Pro667=
NM_000170.3:c.2001T= MANE Select NP_000161.2:p.Pro667=