Canonical Allele Identifier: CA2323623143

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12895912_12895913delinsAC , CM000681.2:g.12895912_12895913delinsAC	GRCh38
NC_000019.9:g.13006726_13006727delinsAC , CM000681.1:g.13006726_13006727delinsAC	GRCh37
NC_000019.8:g.12867726_12867727delinsAC	NCBI36
NG_009292.1:g.9753_9754delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.506-80_506-79delinsAC MANE Select	ENSP00000222214.4:n.506-80_506-79delinsAC...
ENST00000222214.9:c.506-80_506-79delinsAC	ENSP00000222214.4:n.506-80_506-79delinsAC...
ENST00000421816.6:n.484-80_484-79delinsAC
ENST00000585420.5:n.871-80_871-79delinsAC
ENST00000588905.5:c.470-80_470-79delinsAC	ENSP00000465770.1:n.470-80_470-79delinsAC...
ENST00000589039.5:c.443-80_443-79delinsAC	ENSP00000465618.1:n.443-80_443-79delinsAC...
ENST00000590530.5:c.561-80_561-79delinsAC	ENSP00000468452.1:n.561-80_561-79delinsAC...
ENST00000591043.1:n.542-80_542-79delinsAC
ENST00000591470.5:c.506-80_506-79delinsAC	ENSP00000466845.1:n.506-80_506-79delinsAC...
NM_000159.3:c.506-80_506-79delinsAC	NP_000150.1:n.506-80_506-79delinsAC
NM_013976.3:c.506-80_506-79delinsAC	NP_039663.1:n.506-80_506-79delinsAC
NR_102316.1:n.669-80_669-79delinsAC
NR_102317.1:n.922-80_922-79delinsAC
XM_006722721.2:c.506-80_506-79delinsAC	XP_006722784.1:n.506-80_506-79delinsAC
XM_011527899.1:c.506-80_506-79delinsAC	XP_011526201.1:n.506-80_506-79delinsAC
XM_011527900.1:c.506-80_506-79delinsAC	XP_011526202.1:n.506-80_506-79delinsAC
XM_011527899.2:c.506-80_506-79delinsAC	XP_011526201.1:n.506-80_506-79delinsAC
XM_011527900.2:c.506-80_506-79delinsAC	XP_011526202.1:n.506-80_506-79delinsAC
XM_017026580.1:c.506-80_506-79delinsAC	XP_016882069.1:n.506-80_506-79delinsAC
NM_000159.4:c.506-80_506-79delinsAC MANE Select	NP_000150.1:n.506-80_506-79delinsAC
NM_013976.4:c.506-80_506-79delinsAC	NP_039663.1:n.506-80_506-79delinsAC
NM_013976.5:c.506-80_506-79delinsAC	NP_039663.1:n.506-80_506-79delinsAC