Canonical Allele Identifier: CA2582772720
Gene: GCDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12897888_12897891del , CM000681.2:g.12897888_12897891del GRCh38
NC_000019.9:g.13008702_13008705del , CM000681.1:g.13008702_13008705del GRCh37
NC_000019.8:g.12869702_12869705del NCBI36
NG_009292.1:g.11729_11732del
NG_033049.1:g.26384_26387del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.1243+25_1243+28del MANE Select ENSP00000222214.4:n.1243+25_1243+28del
ENST00000222214.9:c.1243+25_1243+28del ENSP00000222214.4:n.1243+25_1243+28del
ENST00000585420.5:n.1573+25_1573+28del
ENST00000590472.5:c.287+25_287+28del
ENST00000590530.5:c.*683+25_*683+28del ENSP00000468452.1:n.*683+25_*683+28del
ENST00000591043.1:n.1553+25_1553+28del
ENST00000591050.1:c.210+25_210+28del
ENST00000591470.5:c.1243+25_1243+28del ENSP00000466845.1:n.1243+25_1243+28del
NM_000159.3:c.1243+25_1243+28del NP_000150.1:n.1243+25_1243+28del
NM_013976.3:c.1243+25_1243+28del NP_039663.1:n.1243+25_1243+28del
NR_102316.1:n.1406+25_1406+28del
NR_102317.1:n.1624+25_1624+28del
XM_006722721.2:c.1243+25_1243+28del XP_006722784.1:n.1243+25_1243+28del
XM_011527899.1:c.1243+25_1243+28del XP_011526201.1:n.1243+25_1243+28del
XM_011527900.1:c.1243+25_1243+28del XP_011526202.1:n.1243+25_1243+28del
XM_011527899.2:c.1243+25_1243+28del XP_011526201.1:n.1243+25_1243+28del
XM_011527900.2:c.1243+25_1243+28del XP_011526202.1:n.1243+25_1243+28del
XM_017026580.1:c.1243+25_1243+28del XP_016882069.1:n.1243+25_1243+28del
NM_000159.4:c.1243+25_1243+28del MANE Select NP_000150.1:n.1243+25_1243+28del
NM_013976.4:c.1243+25_1243+28del NP_039663.1:n.1243+25_1243+28del
NM_013976.5:c.1243+25_1243+28del NP_039663.1:n.1243+25_1243+28del