Canonical Allele Identifier: CA372881970

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558638G>T (hg19) ; chr9:g.6558638G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558638G>T , CM000671.2:g.6558638G>T	GRCh38
NC_000009.11:g.6558638G>T , CM000671.1:g.6558638G>T	GRCh37
NC_000009.10:g.6548638G>T	NCBI36
NG_016397.1:g.92055C>A , LRG_643:g.92055C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1973C>A MANE Select	ENSP00000370737.4:p.Ala658Asp
ENST00000460457.2:n.133C>A
ENST00000638233.1:n.408C>A
ENST00000638661.1:c.173C>A	ENSP00000491369.1:p.Ala58Asp
ENST00000638694.1:n.160C>A
ENST00000639318.1:c.173C>A	ENSP00000491932.1:p.Ala58Asp
ENST00000639364.1:n.1673C>A
ENST00000639443.1:n.1541C>A
ENST00000639954.1:n.1681C>A
ENST00000640208.1:c.173C>A	ENSP00000491895.1:p.Ala58Asp
ENST00000640505.1:n.212C>A
ENST00000640592.1:n.1856C>A
ENST00000321612.6:c.1973C>A	ENSP00000370737.3:p.Ala658Asp
ENST00000460457.1:n.112C>A
NM_000170.2:c.1973C>A , LRG_643t1:c.1973C>A	NP_000161.2:p.Ala658Asp
NM_000170.3:c.1973C>A MANE Select	NP_000161.2:p.Ala658Asp