Canonical Allele Identifier: CA404318631
Gene: GCDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896257G>T , CM000681.2:g.12896257G>T GRCh38
NC_000019.9:g.13007071G>T , CM000681.1:g.13007071G>T GRCh37
NC_000019.8:g.12868071G>T NCBI36
NG_009292.1:g.10098G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.688G>T MANE Select ENSP00000222214.4:p.Asp230Tyr
ENST00000222214.9:c.688G>T ENSP00000222214.4:p.Asp230Tyr
ENST00000421816.6:n.666G>T
ENST00000585420.5:n.1018G>T
ENST00000590530.5:c.*128G>T ENSP00000468452.1:n.*128G>T
ENST00000591043.1:n.724G>T
ENST00000591470.5:c.688G>T ENSP00000466845.1:p.Asp230Tyr
NM_000159.3:c.688G>T NP_000150.1:p.Asp230Tyr
NM_013976.3:c.688G>T NP_039663.1:p.Asp230Tyr
NR_102316.1:n.851G>T
NR_102317.1:n.1069G>T
XM_006722721.2:c.688G>T XP_006722784.1:p.Asp230Tyr
XM_011527899.1:c.688G>T XP_011526201.1:p.Asp230Tyr
XM_011527900.1:c.688G>T XP_011526202.1:p.Asp230Tyr
XM_011527899.2:c.688G>T XP_011526201.1:p.Asp230Tyr
XM_011527900.2:c.688G>T XP_011526202.1:p.Asp230Tyr
XM_017026580.1:c.688G>T XP_016882069.1:p.Asp230Tyr
NM_000159.4:c.688G>T MANE Select NP_000150.1:p.Asp230Tyr
NM_013976.4:c.688G>T NP_039663.1:p.Asp230Tyr
NM_013976.5:c.688G>T NP_039663.1:p.Asp230Tyr