Canonical Allele Identifier: CA404317593
Gene: GCDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12893607T>G , CM000681.2:g.12893607T>G GRCh38
NC_000019.9:g.13004421T>G , CM000681.1:g.13004421T>G GRCh37
NC_000019.8:g.12865421T>G NCBI36
NG_009292.1:g.7448T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.459T>G MANE Select ENSP00000222214.4:p.Tyr153Ter
ENST00000222214.9:c.459T>G ENSP00000222214.4:p.Tyr153Ter
ENST00000421816.6:n.437T>G
ENST00000585420.5:n.824T>G
ENST00000587832.5:n.516T>G
ENST00000588905.5:c.423T>G ENSP00000465770.1:p.Tyr141Ter
ENST00000589039.5:c.396T>G ENSP00000465618.1:p.Tyr132Ter
ENST00000590530.5:c.514T>G ENSP00000468452.1:p.Cys172Gly
ENST00000590627.5:n.824T>G
ENST00000591043.1:n.495T>G
ENST00000591470.5:c.459T>G ENSP00000466845.1:p.Tyr153Ter
NM_000159.3:c.459T>G NP_000150.1:p.Tyr153Ter
NM_013976.3:c.459T>G NP_039663.1:p.Tyr153Ter
NR_102316.1:n.622T>G
NR_102317.1:n.875T>G
XM_006722721.2:c.459T>G XP_006722784.1:p.Tyr153Ter
XM_011527899.1:c.459T>G XP_011526201.1:p.Tyr153Ter
XM_011527900.1:c.459T>G XP_011526202.1:p.Tyr153Ter
XM_011527899.2:c.459T>G XP_011526201.1:p.Tyr153Ter
XM_011527900.2:c.459T>G XP_011526202.1:p.Tyr153Ter
XM_017026580.1:c.459T>G XP_016882069.1:p.Tyr153Ter
NM_000159.4:c.459T>G MANE Select NP_000150.1:p.Tyr153Ter
NM_013976.4:c.459T>G NP_039663.1:p.Tyr153Ter
NM_013976.5:c.459T>G NP_039663.1:p.Tyr153Ter