Canonical Allele Identifier: CA2323623687

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896997_12897000delinsCAGT , CM000681.2:g.12896997_12897000delinsCAGT	GRCh38
NC_000019.9:g.13007811_13007814delinsCAGT , CM000681.1:g.13007811_13007814delinsCAGT	GRCh37
NC_000019.8:g.12868811_12868814delinsCAGT	NCBI36
NG_009292.1:g.10838_10841delinsCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.940_943delinsCAGT MANE Select	ENSP00000222214.4:p.Gln314=
ENST00000222214.9:c.940_943delinsCAGT	ENSP00000222214.4:p.Gln314=
ENST00000421816.6:n.918_921delinsCAGT
ENST00000585420.5:n.1270_1273delinsCAGT
ENST00000590530.5:c.*380_*383delinsCAGT	ENSP00000468452.1:n.*380_*383delinsCAGT
ENST00000591043.1:n.976_979delinsCAGT
ENST00000591470.5:c.940_943delinsCAGT	ENSP00000466845.1:p.Gln314=
NM_000159.3:c.940_943delinsCAGT	NP_000150.1:p.Gln314=
NM_013976.3:c.940_943delinsCAGT	NP_039663.1:p.Gln314=
NR_102316.1:n.1103_1106delinsCAGT
NR_102317.1:n.1321_1324delinsCAGT
XM_006722721.2:c.940_943delinsCAGT	XP_006722784.1:p.Gln314=
XM_011527899.1:c.940_943delinsCAGT	XP_011526201.1:p.Gln314=
XM_011527900.1:c.940_943delinsCAGT	XP_011526202.1:p.Gln314=
XM_011527899.2:c.940_943delinsCAGT	XP_011526201.1:p.Gln314=
XM_011527900.2:c.940_943delinsCAGT	XP_011526202.1:p.Gln314=
XM_017026580.1:c.940_943delinsCAGT	XP_016882069.1:p.Gln314=
NM_000159.4:c.940_943delinsCAGT MANE Select	NP_000150.1:p.Gln314=
NM_013976.4:c.940_943delinsCAGT	NP_039663.1:p.Gln314=
NM_013976.5:c.940_943delinsCAGT	NP_039663.1:p.Gln314=