Canonical Allele Identifier: CA2838791560

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12895988G>T , CM000681.2:g.12895988G>T	GRCh38
NC_000019.9:g.13006802G>T , CM000681.1:g.13006802G>T	GRCh37
NC_000019.8:g.12867802G>T	NCBI36
NG_009292.1:g.9829G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.506-4G>T MANE Select	ENSP00000222214.4:n.506-4G>T
ENST00000222214.9:c.506-4G>T	ENSP00000222214.4:n.506-4G>T
ENST00000421816.6:n.484-4G>T
ENST00000585420.5:n.871-4G>T
ENST00000588905.5:c.470-4G>T	ENSP00000465770.1:n.470-4G>T
ENST00000589039.5:c.443-4G>T	ENSP00000465618.1:n.443-4G>T
ENST00000590530.5:c.561-4G>T	ENSP00000468452.1:n.561-4G>T
ENST00000591043.1:n.542-4G>T
ENST00000591470.5:c.506-4G>T	ENSP00000466845.1:n.506-4G>T
NM_000159.3:c.506-4G>T	NP_000150.1:n.506-4G>T
NM_013976.3:c.506-4G>T	NP_039663.1:n.506-4G>T
NR_102316.1:n.669-4G>T
NR_102317.1:n.922-4G>T
XM_006722721.2:c.506-4G>T	XP_006722784.1:n.506-4G>T
XM_011527899.1:c.506-4G>T	XP_011526201.1:n.506-4G>T
XM_011527900.1:c.506-4G>T	XP_011526202.1:n.506-4G>T
XM_011527899.2:c.506-4G>T	XP_011526201.1:n.506-4G>T
XM_011527900.2:c.506-4G>T	XP_011526202.1:n.506-4G>T
XM_017026580.1:c.506-4G>T	XP_016882069.1:n.506-4G>T
NM_000159.4:c.506-4G>T MANE Select	NP_000150.1:n.506-4G>T
NM_013976.4:c.506-4G>T	NP_039663.1:n.506-4G>T
NM_013976.5:c.506-4G>T	NP_039663.1:n.506-4G>T