Canonical Allele Identifier: CA2323623294

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896200_12896207delinsCCCAGGAT , CM000681.2:g.12896200_12896207delinsCCCAGGAT	GRCh38
NC_000019.9:g.13007014_13007021delinsCCCAGGAT , CM000681.1:g.13007014_13007021delinsCCCAGGAT	GRCh37
NC_000019.8:g.12868014_12868021delinsCCCAGGAT	NCBI36
NG_009292.1:g.10041_10048delinsCCCAGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.636-5_638delinsCCCAGGAT
ENST00000222214.9:c.636-5_638delinsCCCAGGAT
ENST00000421816.6:n.614-5_616delinsCCCAGGAT
ENST00000585420.5:n.1001-40_1001-33delinsCCCAGGAT
ENST00000590530.5:c.*76-5_*78delinsCCCAGGAT
ENST00000591043.1:n.672-5_674delinsCCCAGGAT
ENST00000591470.5:c.636-5_638delinsCCCAGGAT
NM_000159.3:c.636-5_638delinsCCCAGGAT
NM_013976.3:c.636-5_638delinsCCCAGGAT
NR_102316.1:n.799-5_801delinsCCCAGGAT
NR_102317.1:n.1052-40_1052-33delinsCCCAGGAT
XM_006722721.2:c.636-5_638delinsCCCAGGAT
XM_011527899.1:c.636-5_638delinsCCCAGGAT
XM_011527900.1:c.636-5_638delinsCCCAGGAT
XM_011527899.2:c.636-5_638delinsCCCAGGAT
XM_011527900.2:c.636-5_638delinsCCCAGGAT
XM_017026580.1:c.636-5_638delinsCCCAGGAT
NM_000159.4:c.636-5_638delinsCCCAGGAT
NM_013976.4:c.636-5_638delinsCCCAGGAT
NM_013976.5:c.636-5_638delinsCCCAGGAT