Canonical Allele Identifier: CA2782786385
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6555790T>G , CM000671.2:g.6555790T>G GRCh38
NC_000009.11:g.6555790T>G , CM000671.1:g.6555790T>G GRCh37
NC_000009.10:g.6545790T>G NCBI36
NG_016397.1:g.94903A>C , LRG_643:g.94903A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2202+363A>C MANE Select ENSP00000370737.4:n.2202+363A>C
ENST00000638233.1:n.637+363A>C
ENST00000638661.1:c.402+363A>C ENSP00000491369.1:n.402+363A>C
ENST00000638694.1:n.389+363A>C
ENST00000639318.1:c.402+363A>C ENSP00000491932.1:n.402+363A>C
ENST00000639364.1:n.1902+363A>C
ENST00000639443.1:n.1770+363A>C
ENST00000639954.1:n.1910+363A>C
ENST00000640505.1:n.441+363A>C
ENST00000321612.6:c.2202+363A>C ENSP00000370737.3:n.2202+363A>C
NM_000170.2:c.2202+363A>C , LRG_643t1:c.2202+363A>C NP_000161.2:n.2202+363A>C
NM_000170.3:c.2202+363A>C MANE Select NP_000161.2:n.2202+363A>C