Canonical Allele Identifier: CA2576639020

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896122del , CM000681.2:g.12896122del	GRCh38
NC_000019.9:g.13006936del , CM000681.1:g.13006936del	GRCh37
NC_000019.8:g.12867936del	NCBI36
NG_009292.1:g.9963del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.635+1del
ENST00000222214.9:c.635+1del
ENST00000421816.6:n.613+1del
ENST00000585420.5:n.1000+1del
ENST00000590530.5:c.*75+1del
ENST00000591043.1:n.671+1del
ENST00000591470.5:c.635+1del
NM_000159.3:c.635+1del
NM_013976.3:c.635+1del
NR_102316.1:n.798+1del
NR_102317.1:n.1051+1del
XM_006722721.2:c.635+1del
XM_011527899.1:c.635+1del
XM_011527900.1:c.635+1del
XM_011527899.2:c.635+1del
XM_011527900.2:c.635+1del
XM_017026580.1:c.635+1del
NM_000159.4:c.635+1del
NM_013976.4:c.635+1del
NM_013976.5:c.635+1del