Canonical Allele Identifier: CA2323624894

Gene: GCDH SYCE2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12899418_12899419delinsAG , CM000681.2:g.12899418_12899419delinsAG	GRCh38
NC_000019.9:g.13010232_13010233delinsAG , CM000681.1:g.13010232_13010233delinsAG	GRCh37
NC_000019.8:g.12871232_12871233delinsAG	NCBI36
NG_009292.1:g.13259_13260delinsAG
NG_033049.1:g.24854_24855delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1244-50_1244-49delinsAG (GCDH) MANE Select	ENSP00000222214.4:n.1244-50_1244-49delinsAG
ENST00000293695.8:c.613-34_613-33delinsCT (SYCE2) MANE Select	ENSP00000293695.6:n.613-34_613-33delinsCT
ENST00000222214.9:c.1244-50_1244-49delinsAG (GCDH)	ENSP00000222214.4:n.1244-50_1244-49delinsAG
ENST00000293695.7:c.613-34_613-33delinsCT (SYCE2)	ENSP00000293695.6:n.613-34_613-33delinsCT
ENST00000585420.5:n.1574-50_1574-49delinsAG (GCDH)
ENST00000590530.5:c.*684-50_*684-49delinsAG (GCDH)	ENSP00000468452.1:n.*684-50_*684-49delinsAG
ENST00000591043.1:n.1554-50_1554-49delinsAG (GCDH)
ENST00000591050.1:c.210+1555_210+1556delinsAG (GCDH)
ENST00000591470.5:c.1244-50_1244-49delinsAG (GCDH)	ENSP00000466845.1:n.1244-50_1244-49delinsAG
ENST00000592819.1:c.186-34_186-33delinsCT (SYCE2)
NM_000159.3:c.1244-50_1244-49delinsAG (GCDH)	NP_000150.1:n.1244-50_1244-49delinsAG
NM_001105578.1:c.613-34_613-33delinsCT (SYCE2)	NP_001099048.1:n.613-34_613-33delinsCT
NM_013976.3:c.1244-282_1244-281delinsAG (GCDH)	NP_039663.1:n.1244-282_1244-281delinsAG
NR_102316.1:n.1407-50_1407-49delinsAG (GCDH)
NR_102317.1:n.1625-50_1625-49delinsAG (GCDH)
XM_005259848.3:c.*23-34_*23-33delinsCT (SYCE2)	XP_005259905.1:n.*23-34_*23-33delinsCT
XM_006722721.2:c.1244-816_1244-815delinsAG (GCDH)	XP_006722784.1:n.1244-816_1244-815delinsAG
XM_011527882.1:c.610-34_610-33delinsCT (SYCE2)	XP_011526184.1:n.610-34_610-33delinsCT
XM_011527883.1:c.*23-34_*23-33delinsCT (SYCE2)	XP_011526185.1:n.*23-34_*23-33delinsCT
XM_011527899.1:c.1243+1555_1243+1556delinsAG (GCDH)	XP_011526201.1:n.1243+1555_1243+1556delinsAG
XM_011527900.1:c.1244-816_1244-815delinsAG (GCDH)	XP_011526202.1:n.1244-816_1244-815delinsAG
XM_005259848.4:c.*23-34_*23-33delinsCT (SYCE2)	XP_005259905.1:n.*23-34_*23-33delinsCT
XM_011527882.2:c.610-34_610-33delinsCT (SYCE2)	XP_011526184.1:n.610-34_610-33delinsCT
XM_011527883.2:c.*23-34_*23-33delinsCT (SYCE2)	XP_011526185.1:n.*23-34_*23-33delinsCT
XM_011527899.2:c.1243+1555_1243+1556delinsAG (GCDH)	XP_011526201.1:n.1243+1555_1243+1556delinsAG
XM_011527900.2:c.1244-816_1244-815delinsAG (GCDH)	XP_011526202.1:n.1244-816_1244-815delinsAG
XM_017026580.1:c.1244-816_1244-815delinsAG (GCDH)	XP_016882069.1:n.1244-816_1244-815delinsAG
NM_000159.4:c.1244-50_1244-49delinsAG (GCDH) MANE Select	NP_000150.1:n.1244-50_1244-49delinsAG
NM_001105578.2:c.613-34_613-33delinsCT (SYCE2) MANE Select	NP_001099048.1:n.613-34_613-33delinsCT
NM_013976.4:c.1244-282_1244-281delinsAG (GCDH)	NP_039663.1:n.1244-282_1244-281delinsAG
NM_013976.5:c.1244-282_1244-281delinsAG (GCDH)	NP_039663.1:n.1244-282_1244-281delinsAG