Canonical Allele Identifier: CA2582772028

Gene: GCDH

Linked Data

• gnomAD v4: 19-12895901-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12895901T>G , CM000681.2:g.12895901T>G	GRCh38
NC_000019.9:g.13006715T>G , CM000681.1:g.13006715T>G	GRCh37
NC_000019.8:g.12867715T>G	NCBI36
NG_009292.1:g.9742T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.506-91T>G MANE Select	ENSP00000222214.4:n.506-91T>G
ENST00000222214.9:c.506-91T>G	ENSP00000222214.4:n.506-91T>G
ENST00000421816.6:n.484-91T>G
ENST00000585420.5:n.871-91T>G
ENST00000588905.5:c.470-91T>G	ENSP00000465770.1:n.470-91T>G
ENST00000589039.5:c.443-91T>G	ENSP00000465618.1:n.443-91T>G
ENST00000590530.5:c.561-91T>G	ENSP00000468452.1:n.561-91T>G
ENST00000591043.1:n.542-91T>G
ENST00000591470.5:c.506-91T>G	ENSP00000466845.1:n.506-91T>G
NM_000159.3:c.506-91T>G	NP_000150.1:n.506-91T>G
NM_013976.3:c.506-91T>G	NP_039663.1:n.506-91T>G
NR_102316.1:n.669-91T>G
NR_102317.1:n.922-91T>G
XM_006722721.2:c.506-91T>G	XP_006722784.1:n.506-91T>G
XM_011527899.1:c.506-91T>G	XP_011526201.1:n.506-91T>G
XM_011527900.1:c.506-91T>G	XP_011526202.1:n.506-91T>G
XM_011527899.2:c.506-91T>G	XP_011526201.1:n.506-91T>G
XM_011527900.2:c.506-91T>G	XP_011526202.1:n.506-91T>G
XM_017026580.1:c.506-91T>G	XP_016882069.1:n.506-91T>G
NM_000159.4:c.506-91T>G MANE Select	NP_000150.1:n.506-91T>G
NM_013976.4:c.506-91T>G	NP_039663.1:n.506-91T>G
NM_013976.5:c.506-91T>G	NP_039663.1:n.506-91T>G