Canonical Allele Identifier: CA16041973
Gene: GCDH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896930del , CM000681.2:g.12896930del GRCh38
NC_000019.9:g.13007744del , CM000681.1:g.13007744del GRCh37
NC_000019.8:g.12868744del NCBI36
NG_009292.1:g.10771del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.873del MANE Select ENSP00000222214.4:p.Asn291LysfsTer?
ENST00000222214.9:c.873del ENSP00000222214.4:p.Asn291LysfsTer?
ENST00000421816.6:n.851del
ENST00000585420.5:n.1203del
ENST00000590530.5:c.*313del ENSP00000468452.1:n.*313del
ENST00000591043.1:n.909del
ENST00000591470.5:c.873del ENSP00000466845.1:p.Asn291LysfsTer?
NM_000159.3:c.873del NP_000150.1:p.Asn291LysfsTer?
NM_013976.3:c.873del NP_039663.1:p.Asn291LysfsTer?
NR_102316.1:n.1036del
NR_102317.1:n.1254del
XM_006722721.2:c.873del XP_006722784.1:p.Asn291LysfsTer?
XM_011527899.1:c.873del XP_011526201.1:p.Asn291LysfsTer?
XM_011527900.1:c.873del XP_011526202.1:p.Asn291LysfsTer?
XM_011527899.2:c.873del XP_011526201.1:p.Asn291LysfsTer?
XM_011527900.2:c.873del XP_011526202.1:p.Asn291LysfsTer?
XM_017026580.1:c.873del XP_016882069.1:p.Asn291LysfsTer?
NM_000159.4:c.873del MANE Select NP_000150.1:p.Asn291LysfsTer?
NM_013976.4:c.873del NP_039663.1:p.Asn291LysfsTer?
NM_013976.5:c.873del NP_039663.1:p.Asn291LysfsTer?
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