Canonical Allele Identifier: CA2576638977

Gene: GCDH

Linked Data

• gnomAD v4: 19-12895918-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12895918C>A , CM000681.2:g.12895918C>A	GRCh38
NC_000019.9:g.13006732C>A , CM000681.1:g.13006732C>A	GRCh37
NC_000019.8:g.12867732C>A	NCBI36
NG_009292.1:g.9759C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.506-74C>A MANE Select	ENSP00000222214.4:n.506-74C>A
ENST00000222214.9:c.506-74C>A	ENSP00000222214.4:n.506-74C>A
ENST00000421816.6:n.484-74C>A
ENST00000585420.5:n.871-74C>A
ENST00000588905.5:c.470-74C>A	ENSP00000465770.1:n.470-74C>A
ENST00000589039.5:c.443-74C>A	ENSP00000465618.1:n.443-74C>A
ENST00000590530.5:c.561-74C>A	ENSP00000468452.1:n.561-74C>A
ENST00000591043.1:n.542-74C>A
ENST00000591470.5:c.506-74C>A	ENSP00000466845.1:n.506-74C>A
NM_000159.3:c.506-74C>A	NP_000150.1:n.506-74C>A
NM_013976.3:c.506-74C>A	NP_039663.1:n.506-74C>A
NR_102316.1:n.669-74C>A
NR_102317.1:n.922-74C>A
XM_006722721.2:c.506-74C>A	XP_006722784.1:n.506-74C>A
XM_011527899.1:c.506-74C>A	XP_011526201.1:n.506-74C>A
XM_011527900.1:c.506-74C>A	XP_011526202.1:n.506-74C>A
XM_011527899.2:c.506-74C>A	XP_011526201.1:n.506-74C>A
XM_011527900.2:c.506-74C>A	XP_011526202.1:n.506-74C>A
XM_017026580.1:c.506-74C>A	XP_016882069.1:n.506-74C>A
NM_000159.4:c.506-74C>A MANE Select	NP_000150.1:n.506-74C>A
NM_013976.4:c.506-74C>A	NP_039663.1:n.506-74C>A
NM_013976.5:c.506-74C>A	NP_039663.1:n.506-74C>A