Canonical Allele Identifier: CA2323623342

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896296_12896297delinsCG , CM000681.2:g.12896296_12896297delinsCG	GRCh38
NC_000019.9:g.13007110_13007111delinsCG , CM000681.1:g.13007110_13007111delinsCG	GRCh37
NC_000019.8:g.12868110_12868111delinsCG	NCBI36
NG_009292.1:g.10137_10138delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.727_728delinsCG MANE Select	ENSP00000222214.4:p.Arg243=
ENST00000222214.9:c.727_728delinsCG	ENSP00000222214.4:p.Arg243=
ENST00000421816.6:n.705_706delinsCG
ENST00000585420.5:n.1057_1058delinsCG
ENST00000590530.5:c.*167_*168delinsCG	ENSP00000468452.1:n.*167_*168delinsCG
ENST00000591043.1:n.763_764delinsCG
ENST00000591470.5:c.727_728delinsCG	ENSP00000466845.1:p.Arg243=
NM_000159.3:c.727_728delinsCG	NP_000150.1:p.Arg243=
NM_013976.3:c.727_728delinsCG	NP_039663.1:p.Arg243=
NR_102316.1:n.890_891delinsCG
NR_102317.1:n.1108_1109delinsCG
XM_006722721.2:c.727_728delinsCG	XP_006722784.1:p.Arg243=
XM_011527899.1:c.727_728delinsCG	XP_011526201.1:p.Arg243=
XM_011527900.1:c.727_728delinsCG	XP_011526202.1:p.Arg243=
XM_011527899.2:c.727_728delinsCG	XP_011526201.1:p.Arg243=
XM_011527900.2:c.727_728delinsCG	XP_011526202.1:p.Arg243=
XM_017026580.1:c.727_728delinsCG	XP_016882069.1:p.Arg243=
NM_000159.4:c.727_728delinsCG MANE Select	NP_000150.1:p.Arg243=
NM_013976.4:c.727_728delinsCG	NP_039663.1:p.Arg243=
NM_013976.5:c.727_728delinsCG	NP_039663.1:p.Arg243=