Canonical Allele Identifier: CA2582771431

Gene: GCDH

Linked Data

• gnomAD v4: 19-12893393-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893393T>G , CM000681.2:g.12893393T>G	GRCh38
NC_000019.9:g.13004207T>G , CM000681.1:g.13004207T>G	GRCh37
NC_000019.8:g.12865207T>G	NCBI36
NG_009292.1:g.7234T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.335-90T>G MANE Select	ENSP00000222214.4:n.335-90T>G
ENST00000222214.9:c.335-90T>G	ENSP00000222214.4:n.335-90T>G
ENST00000421816.6:n.313-90T>G
ENST00000585420.5:n.700-90T>G
ENST00000587072.1:c.383-90T>G	ENSP00000468584.1:n.383-90T>G
ENST00000587832.5:n.392-90T>G
ENST00000588905.5:c.299-90T>G	ENSP00000465770.1:n.299-90T>G
ENST00000589039.5:c.272-90T>G	ENSP00000465618.1:n.272-90T>G
ENST00000590530.5:c.390-90T>G	ENSP00000468452.1:n.390-90T>G
ENST00000590627.5:n.700-90T>G
ENST00000591043.1:n.371-90T>G
ENST00000591470.5:c.335-90T>G	ENSP00000466845.1:n.335-90T>G
NM_000159.3:c.335-90T>G	NP_000150.1:n.335-90T>G
NM_013976.3:c.335-90T>G	NP_039663.1:n.335-90T>G
NR_102316.1:n.498-90T>G
NR_102317.1:n.751-90T>G
XM_006722721.2:c.335-90T>G	XP_006722784.1:n.335-90T>G
XM_011527899.1:c.335-90T>G	XP_011526201.1:n.335-90T>G
XM_011527900.1:c.335-90T>G	XP_011526202.1:n.335-90T>G
XM_011527899.2:c.335-90T>G	XP_011526201.1:n.335-90T>G
XM_011527900.2:c.335-90T>G	XP_011526202.1:n.335-90T>G
XM_017026580.1:c.335-90T>G	XP_016882069.1:n.335-90T>G
NM_000159.4:c.335-90T>G MANE Select	NP_000150.1:n.335-90T>G
NM_013976.4:c.335-90T>G	NP_039663.1:n.335-90T>G
NM_013976.5:c.335-90T>G	NP_039663.1:n.335-90T>G