Canonical Allele Identifier: CA2582772341

Gene: GCDH

Linked Data

• gnomAD v4: 19-12897022-GGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897023_12897025del , CM000681.2:g.12897023_12897025del	GRCh38
NC_000019.9:g.13007837_13007839del , CM000681.1:g.13007837_13007839del	GRCh37
NC_000019.8:g.12868837_12868839del	NCBI36
NG_009292.1:g.10864_10866del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.956+10_956+12del MANE Select	ENSP00000222214.4:n.956+10_956+12del
ENST00000222214.9:c.956+10_956+12del	ENSP00000222214.4:n.956+10_956+12del
ENST00000421816.6:n.934+10_934+12del
ENST00000585420.5:n.1286+10_1286+12del
ENST00000590530.5:c.*396+10_*396+12del	ENSP00000468452.1:n.*396+10_*396+12del
ENST00000591043.1:n.992+10_992+12del
ENST00000591470.5:c.956+10_956+12del	ENSP00000466845.1:n.956+10_956+12del
NM_000159.3:c.956+10_956+12del	NP_000150.1:n.956+10_956+12del
NM_013976.3:c.956+10_956+12del	NP_039663.1:n.956+10_956+12del
NR_102316.1:n.1119+10_1119+12del
NR_102317.1:n.1337+10_1337+12del
XM_006722721.2:c.956+10_956+12del	XP_006722784.1:n.956+10_956+12del
XM_011527899.1:c.956+10_956+12del	XP_011526201.1:n.956+10_956+12del
XM_011527900.1:c.956+10_956+12del	XP_011526202.1:n.956+10_956+12del
XM_011527899.2:c.956+10_956+12del	XP_011526201.1:n.956+10_956+12del
XM_011527900.2:c.956+10_956+12del	XP_011526202.1:n.956+10_956+12del
XM_017026580.1:c.956+10_956+12del	XP_016882069.1:n.956+10_956+12del
NM_000159.4:c.956+10_956+12del MANE Select	NP_000150.1:n.956+10_956+12del
NM_013976.4:c.956+10_956+12del	NP_039663.1:n.956+10_956+12del
NM_013976.5:c.956+10_956+12del	NP_039663.1:n.956+10_956+12del