Canonical Allele Identifier: CA2695228348
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896884_12896911del , CM000681.2:g.12896884_12896911del GRCh38
NC_000019.9:g.13007698_13007725del , CM000681.1:g.13007698_13007725del GRCh37
NC_000019.8:g.12868698_12868725del NCBI36
NG_009292.1:g.10725_10752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.853-26_854del
ENST00000222214.9:c.853-26_854del
ENST00000421816.6:n.831-26_832del
ENST00000585420.5:n.1183-26_1184del
ENST00000590530.5:c.*293-26_*294del
ENST00000591043.1:n.889-26_890del
ENST00000591470.5:c.853-26_854del
NM_000159.3:c.853-26_854del
NM_013976.3:c.853-26_854del
NR_102316.1:n.1016-26_1017del
NR_102317.1:n.1234-26_1235del
XM_006722721.2:c.853-26_854del
XM_011527899.1:c.853-26_854del
XM_011527900.1:c.853-26_854del
XM_011527899.2:c.853-26_854del
XM_011527900.2:c.853-26_854del
XM_017026580.1:c.853-26_854del
NM_000159.4:c.853-26_854del
NM_013976.4:c.853-26_854del
NM_013976.5:c.853-26_854del