Canonical Allele Identifier: CA1830496420
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558639C= , CM000671.2:g.6558639C= GRCh38
NC_000009.11:g.6558639C= , CM000671.1:g.6558639C= GRCh37
NC_000009.10:g.6548639C= NCBI36
NG_016397.1:g.92054G= , LRG_643:g.92054G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1972G= MANE Select ENSP00000370737.4:p.Ala658=
ENST00000460457.2:n.132G=
ENST00000638233.1:n.407G=
ENST00000638661.1:c.172G= ENSP00000491369.1:p.Ala58=
ENST00000638694.1:n.159G=
ENST00000639318.1:c.172G= ENSP00000491932.1:p.Ala58=
ENST00000639364.1:n.1672G=
ENST00000639443.1:n.1540G=
ENST00000639954.1:n.1680G=
ENST00000640208.1:c.172G= ENSP00000491895.1:p.Ala58=
ENST00000640505.1:n.211G=
ENST00000640592.1:n.1855G=
ENST00000321612.6:c.1972G= ENSP00000370737.3:p.Ala658=
ENST00000460457.1:n.111G=
NM_000170.2:c.1972G= , LRG_643t1:c.1972G= NP_000161.2:p.Ala658=
NM_000170.3:c.1972G= MANE Select NP_000161.2:p.Ala658=