Canonical Allele Identifier: CA865926643

Gene: GLDC

Linked Data

• dbSNP Id: rs1412684613
• MyVariant Identifiers: chr9:g.6593011C>T (hg19) ; chr9:g.6593011C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6593011C>T , CM000671.2:g.6593011C>T	GRCh38
NC_000009.11:g.6593011C>T , CM000671.1:g.6593011C>T	GRCh37
NC_000009.10:g.6583011C>T	NCBI36
NG_016397.1:g.57682G>A , LRG_643:g.57682G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1262-21G>A MANE Select	ENSP00000370737.4:n.1262-21G>A
ENST00000639364.1:n.962-21G>A
ENST00000639443.1:n.830-21G>A
ENST00000639493.1:n.414-21G>A
ENST00000639954.1:n.970-21G>A
ENST00000640592.1:n.1145-21G>A
ENST00000640703.1:n.84G>A
ENST00000321612.6:c.1262-21G>A	ENSP00000370737.3:n.1262-21G>A
ENST00000463305.1:n.346-21G>A
NM_000170.2:c.1262-21G>A , LRG_643t1:c.1262-21G>A	NP_000161.2:n.1262-21G>A
NM_000170.3:c.1262-21G>A MANE Select	NP_000161.2:n.1262-21G>A