Canonical Allele Identifier: CA2582772086

Gene: GCDH

Linked Data

• gnomAD v4: 19-12896154-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896155_12896156del , CM000681.2:g.12896155_12896156del	GRCh38
NC_000019.9:g.13006969_13006970del , CM000681.1:g.13006969_13006970del	GRCh37
NC_000019.8:g.12867969_12867970del	NCBI36
NG_009292.1:g.9996_9997del

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.635+34_635+35del MANE Select	ENSP00000222214.4:n.635+34_635+35del
ENST00000222214.9:c.635+34_635+35del	ENSP00000222214.4:n.635+34_635+35del
ENST00000421816.6:n.613+34_613+35del
ENST00000585420.5:n.1000+34_1000+35del
ENST00000590530.5:c.*75+34_*75+35del	ENSP00000468452.1:n.*75+34_*75+35del
ENST00000591043.1:n.671+34_671+35del
ENST00000591470.5:c.635+34_635+35del	ENSP00000466845.1:n.635+34_635+35del
NM_000159.3:c.635+34_635+35del	NP_000150.1:n.635+34_635+35del
NM_013976.3:c.635+34_635+35del	NP_039663.1:n.635+34_635+35del
NR_102316.1:n.798+34_798+35del
NR_102317.1:n.1051+34_1051+35del
XM_006722721.2:c.635+34_635+35del	XP_006722784.1:n.635+34_635+35del
XM_011527899.1:c.635+34_635+35del	XP_011526201.1:n.635+34_635+35del
XM_011527900.1:c.635+34_635+35del	XP_011526202.1:n.635+34_635+35del
XM_011527899.2:c.635+34_635+35del	XP_011526201.1:n.635+34_635+35del
XM_011527900.2:c.635+34_635+35del	XP_011526202.1:n.635+34_635+35del
XM_017026580.1:c.635+34_635+35del	XP_016882069.1:n.635+34_635+35del
NM_000159.4:c.635+34_635+35del MANE Select	NP_000150.1:n.635+34_635+35del
NM_013976.4:c.635+34_635+35del	NP_039663.1:n.635+34_635+35del
NM_013976.5:c.635+34_635+35del	NP_039663.1:n.635+34_635+35del