Canonical Allele Identifier: CA2576639290

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12899286del , CM000681.2:g.12899286del GRCh38
NC_000019.9:g.13010100del , CM000681.1:g.13010100del GRCh37
NC_000019.8:g.12871100del NCBI36
NG_009292.1:g.13127del
NG_033049.1:g.24988del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.1244-182del (GCDH) MANE Select ENSP00000222214.4:n.1244-182del
ENST00000293695.8:c.*56del (SYCE2) MANE Select ENSP00000293695.6:n.*56del
ENST00000222214.9:c.1244-182del (GCDH) ENSP00000222214.4:n.1244-182del
ENST00000293695.7:c.*56del (SYCE2) ENSP00000293695.6:n.*56del
ENST00000585420.5:n.1574-182del (GCDH)
ENST00000590530.5:c.*684-182del (GCDH) ENSP00000468452.1:n.*684-182del
ENST00000591043.1:n.1554-182del (GCDH)
ENST00000591050.1:c.210+1423del (GCDH)
ENST00000591470.5:c.1244-182del (GCDH) ENSP00000466845.1:n.1244-182del
ENST00000592819.1:c.286del (SYCE2)
NM_000159.3:c.1244-182del (GCDH) NP_000150.1:n.1244-182del
NM_001105578.1:c.*56del (SYCE2) NP_001099048.1:n.*56del
NM_013976.3:c.1244-414del (GCDH) NP_039663.1:n.1244-414del
NR_102316.1:n.1407-182del (GCDH)
NR_102317.1:n.1625-182del (GCDH)
XM_006722721.2:c.1244-948del (GCDH) XP_006722784.1:n.1244-948del
XM_011527882.1:c.*56del (SYCE2) XP_011526184.1:n.*56del
XM_011527883.1:c.*123del (SYCE2) XP_011526185.1:n.*123del
XM_011527899.1:c.1243+1423del (GCDH) XP_011526201.1:n.1243+1423del
XM_011527900.1:c.1244-948del (GCDH) XP_011526202.1:n.1244-948del
XM_005259848.4:c.*123del (SYCE2) XP_005259905.1:n.*123del
XM_011527882.2:c.*56del (SYCE2) XP_011526184.1:n.*56del
XM_011527883.2:c.*123del (SYCE2) XP_011526185.1:n.*123del
XM_011527899.2:c.1243+1423del (GCDH) XP_011526201.1:n.1243+1423del
XM_011527900.2:c.1244-948del (GCDH) XP_011526202.1:n.1244-948del
XM_017026580.1:c.1244-948del (GCDH) XP_016882069.1:n.1244-948del
NM_000159.4:c.1244-182del (GCDH) MANE Select NP_000150.1:n.1244-182del
NM_001105578.2:c.*56del (SYCE2) MANE Select NP_001099048.1:n.*56del
NM_013976.4:c.1244-414del (GCDH) NP_039663.1:n.1244-414del
NM_013976.5:c.1244-414del (GCDH) NP_039663.1:n.1244-414del