Canonical Allele Identifier: CA9234482
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 529442
dbSNP Id: rs751583656

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896339G>A , CM000681.2:g.12896339G>A GRCh38
NC_000019.9:g.13007153G>A , CM000681.1:g.13007153G>A GRCh37
NC_000019.8:g.12868153G>A NCBI36
NG_009292.1:g.10180G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.770G>A MANE Select ENSP00000222214.4:p.Arg257Gln
ENST00000222214.9:c.770G>A ENSP00000222214.4:p.Arg257Gln
ENST00000421816.6:n.748G>A
ENST00000585420.5:n.1100G>A
ENST00000590530.5:c.*210G>A ENSP00000468452.1:n.*210G>A
ENST00000591043.1:n.806G>A
ENST00000591470.5:c.770G>A ENSP00000466845.1:p.Arg257Gln
NM_000159.3:c.770G>A NP_000150.1:p.Arg257Gln
NM_013976.3:c.770G>A NP_039663.1:p.Arg257Gln
NR_102316.1:n.933G>A
NR_102317.1:n.1151G>A
XM_006722721.2:c.770G>A XP_006722784.1:p.Arg257Gln
XM_011527899.1:c.770G>A XP_011526201.1:p.Arg257Gln
XM_011527900.1:c.770G>A XP_011526202.1:p.Arg257Gln
XM_011527899.2:c.770G>A XP_011526201.1:p.Arg257Gln
XM_011527900.2:c.770G>A XP_011526202.1:p.Arg257Gln
XM_017026580.1:c.770G>A XP_016882069.1:p.Arg257Gln
NM_000159.4:c.770G>A MANE Select NP_000150.1:p.Arg257Gln
NM_013976.4:c.770G>A NP_039663.1:p.Arg257Gln
NM_013976.5:c.770G>A NP_039663.1:p.Arg257Gln