Canonical Allele Identifier: CA1830496775
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558968T= , CM000671.2:g.6558968T= GRCh38
NC_000009.11:g.6558968T= , CM000671.1:g.6558968T= GRCh37
NC_000009.10:g.6548968T= NCBI36
NG_016397.1:g.91725A= , LRG_643:g.91725A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1927-284A= MANE Select ENSP00000370737.4:n.1927-284A=
ENST00000460457.2:n.87-284A=
ENST00000638233.1:n.362-284A=
ENST00000638661.1:c.127-284A= ENSP00000491369.1:n.127-284A=
ENST00000638694.1:n.114-284A=
ENST00000639318.1:c.127-284A= ENSP00000491932.1:n.127-284A=
ENST00000639364.1:n.1627-284A=
ENST00000639443.1:n.1495-284A=
ENST00000639954.1:n.1635-284A=
ENST00000640208.1:c.127-284A= ENSP00000491895.1:n.127-284A=
ENST00000640505.1:n.166-284A=
ENST00000640592.1:n.1810-284A=
ENST00000321612.6:c.1927-284A= ENSP00000370737.3:n.1927-284A=
ENST00000460457.1:n.66-284A=
NM_000170.2:c.1927-284A= , LRG_643t1:c.1927-284A= NP_000161.2:n.1927-284A=
NM_000170.3:c.1927-284A= MANE Select NP_000161.2:n.1927-284A=