Canonical Allele Identifier: CA1830493343
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556153C= , CM000671.2:g.6556153C= GRCh38
NC_000009.11:g.6556153C= , CM000671.1:g.6556153C= GRCh37
NC_000009.10:g.6546153C= NCBI36
NG_016397.1:g.94540G= , LRG_643:g.94540G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2202G= MANE Select ENSP00000370737.4:p.Gln734=
ENST00000638233.1:n.637G=
ENST00000638661.1:c.402G= ENSP00000491369.1:p.Gln134=
ENST00000638694.1:n.389G=
ENST00000639318.1:c.402G= ENSP00000491932.1:p.Gln134=
ENST00000639364.1:n.1902G=
ENST00000639443.1:n.1770G=
ENST00000639954.1:n.1910G=
ENST00000640505.1:n.441G=
ENST00000321612.6:c.2202G= ENSP00000370737.3:p.Gln734=
NM_000170.2:c.2202G= , LRG_643t1:c.2202G= NP_000161.2:p.Gln734=
NM_000170.3:c.2202G= MANE Select NP_000161.2:p.Gln734=