Canonical Allele Identifier: CA2323624855

Gene: GCDH SYCE2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12899329_12899330delinsTC , CM000681.2:g.12899329_12899330delinsTC	GRCh38
NC_000019.9:g.13010143_13010144delinsTC , CM000681.1:g.13010143_13010144delinsTC	GRCh37
NC_000019.8:g.12871143_12871144delinsTC	NCBI36
NG_009292.1:g.13170_13171delinsTC
NG_033049.1:g.24943_24944delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1244-139_1244-138delinsTC (GCDH) MANE Select	ENSP00000222214.4:n.1244-139_1244-138delinsTC
ENST00000293695.8:c.*11_*12delinsGA (SYCE2) MANE Select	ENSP00000293695.6:n.*11_*12delinsGA
ENST00000222214.9:c.1244-139_1244-138delinsTC (GCDH)	ENSP00000222214.4:n.1244-139_1244-138delinsTC
ENST00000293695.7:c.*11_*12delinsGA (SYCE2)	ENSP00000293695.6:n.*11_*12delinsGA
ENST00000585420.5:n.1574-139_1574-138delinsTC (GCDH)
ENST00000590530.5:c.*684-139_*684-138delinsTC (GCDH)	ENSP00000468452.1:n.*684-139_*684-138delinsTC
ENST00000591043.1:n.1554-139_1554-138delinsTC (GCDH)
ENST00000591050.1:c.210+1466_210+1467delinsTC (GCDH)
ENST00000591470.5:c.1244-139_1244-138delinsTC (GCDH)	ENSP00000466845.1:n.1244-139_1244-138delinsTC
ENST00000592819.1:c.241_242delinsGA (SYCE2)
NM_000159.3:c.1244-139_1244-138delinsTC (GCDH)	NP_000150.1:n.1244-139_1244-138delinsTC
NM_001105578.1:c.*11_*12delinsGA (SYCE2)	NP_001099048.1:n.*11_*12delinsGA
NM_013976.3:c.1244-371_1244-370delinsTC (GCDH)	NP_039663.1:n.1244-371_1244-370delinsTC
NR_102316.1:n.1407-139_1407-138delinsTC (GCDH)
NR_102317.1:n.1625-139_1625-138delinsTC (GCDH)
XM_005259848.3:c.*78_*79delinsGA (SYCE2)	XP_005259905.1:n.*78_*79delinsGA
XM_006722721.2:c.1244-905_1244-904delinsTC (GCDH)	XP_006722784.1:n.1244-905_1244-904delinsTC
XM_011527882.1:c.*11_*12delinsGA (SYCE2)	XP_011526184.1:n.*11_*12delinsGA
XM_011527883.1:c.*78_*79delinsGA (SYCE2)	XP_011526185.1:n.*78_*79delinsGA
XM_011527899.1:c.1243+1466_1243+1467delinsTC (GCDH)	XP_011526201.1:n.1243+1466_1243+1467delinsTC
XM_011527900.1:c.1244-905_1244-904delinsTC (GCDH)	XP_011526202.1:n.1244-905_1244-904delinsTC
XM_005259848.4:c.*78_*79delinsGA (SYCE2)	XP_005259905.1:n.*78_*79delinsGA
XM_011527882.2:c.*11_*12delinsGA (SYCE2)	XP_011526184.1:n.*11_*12delinsGA
XM_011527883.2:c.*78_*79delinsGA (SYCE2)	XP_011526185.1:n.*78_*79delinsGA
XM_011527899.2:c.1243+1466_1243+1467delinsTC (GCDH)	XP_011526201.1:n.1243+1466_1243+1467delinsTC
XM_011527900.2:c.1244-905_1244-904delinsTC (GCDH)	XP_011526202.1:n.1244-905_1244-904delinsTC
XM_017026580.1:c.1244-905_1244-904delinsTC (GCDH)	XP_016882069.1:n.1244-905_1244-904delinsTC
NM_000159.4:c.1244-139_1244-138delinsTC (GCDH) MANE Select	NP_000150.1:n.1244-139_1244-138delinsTC
NM_001105578.2:c.*11_*12delinsGA (SYCE2) MANE Select	NP_001099048.1:n.*11_*12delinsGA
NM_013976.4:c.1244-371_1244-370delinsTC (GCDH)	NP_039663.1:n.1244-371_1244-370delinsTC
NM_013976.5:c.1244-371_1244-370delinsTC (GCDH)	NP_039663.1:n.1244-371_1244-370delinsTC