Canonical Allele Identifier: CA2323624865

Gene: GCDH SYCE2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12899347_12899353delinsTTCACCA , CM000681.2:g.12899347_12899353delinsTTCACCA	GRCh38
NC_000019.9:g.13010161_13010167delinsTTCACCA , CM000681.1:g.13010161_13010167delinsTTCACCA	GRCh37
NC_000019.8:g.12871161_12871167delinsTTCACCA	NCBI36
NG_009292.1:g.13188_13194delinsTTCACCA
NG_033049.1:g.24920_24926delinsTGGTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1244-121_1244-115delinsTTCACCA (GCDH) MANE Select	ENSP00000222214.4:n.1244-121_1244-115delinsTTCACCA
ENST00000293695.8:c.645_651delinsTGGTGAA (SYCE2) MANE Select	ENSP00000293695.6:p.Asp215=
ENST00000222214.9:c.1244-121_1244-115delinsTTCACCA (GCDH)	ENSP00000222214.4:n.1244-121_1244-115delinsTTCACCA
ENST00000293695.7:c.645_651delinsTGGTGAA (SYCE2)	ENSP00000293695.6:p.Asp215=
ENST00000585420.5:n.1574-121_1574-115delinsTTCACCA (GCDH)
ENST00000590530.5:c.*684-121_*684-115delinsTTCACCA (GCDH)	ENSP00000468452.1:n.*684-121_*684-115delinsTTCACCA
ENST00000591043.1:n.1554-121_1554-115delinsTTCACCA (GCDH)
ENST00000591050.1:c.210+1484_210+1490delinsTTCACCA (GCDH)
ENST00000591470.5:c.1244-121_1244-115delinsTTCACCA (GCDH)	ENSP00000466845.1:n.1244-121_1244-115delinsTTCACCA
ENST00000592819.1:c.218_224delinsTGGTGAA (SYCE2)
NM_000159.3:c.1244-121_1244-115delinsTTCACCA (GCDH)	NP_000150.1:n.1244-121_1244-115delinsTTCACCA
NM_001105578.1:c.645_651delinsTGGTGAA (SYCE2)	NP_001099048.1:p.Asp215=
NM_013976.3:c.1244-353_1244-347delinsTTCACCA (GCDH)	NP_039663.1:n.1244-353_1244-347delinsTTCACCA
NR_102316.1:n.1407-121_1407-115delinsTTCACCA (GCDH)
NR_102317.1:n.1625-121_1625-115delinsTTCACCA (GCDH)
XM_005259848.3:c.*55_*61delinsTGGTGAA (SYCE2)	XP_005259905.1:n.*55_*61delinsTGGTGAA
XM_006722721.2:c.1244-887_1244-881delinsTTCACCA (GCDH)	XP_006722784.1:n.1244-887_1244-881delinsTTCACCA
XM_011527882.1:c.642_648delinsTGGTGAA (SYCE2)	XP_011526184.1:p.Asp214=
XM_011527883.1:c.*55_*61delinsTGGTGAA (SYCE2)	XP_011526185.1:n.*55_*61delinsTGGTGAA
XM_011527899.1:c.1243+1484_1243+1490delinsTTCACCA (GCDH)	XP_011526201.1:n.1243+1484_1243+1490delinsTTCACCA
XM_011527900.1:c.1244-887_1244-881delinsTTCACCA (GCDH)	XP_011526202.1:n.1244-887_1244-881delinsTTCACCA
XM_005259848.4:c.*55_*61delinsTGGTGAA (SYCE2)	XP_005259905.1:n.*55_*61delinsTGGTGAA
XM_011527882.2:c.642_648delinsTGGTGAA (SYCE2)	XP_011526184.1:p.Asp214=
XM_011527883.2:c.*55_*61delinsTGGTGAA (SYCE2)	XP_011526185.1:n.*55_*61delinsTGGTGAA
XM_011527899.2:c.1243+1484_1243+1490delinsTTCACCA (GCDH)	XP_011526201.1:n.1243+1484_1243+1490delinsTTCACCA
XM_011527900.2:c.1244-887_1244-881delinsTTCACCA (GCDH)	XP_011526202.1:n.1244-887_1244-881delinsTTCACCA
XM_017026580.1:c.1244-887_1244-881delinsTTCACCA (GCDH)	XP_016882069.1:n.1244-887_1244-881delinsTTCACCA
NM_000159.4:c.1244-121_1244-115delinsTTCACCA (GCDH) MANE Select	NP_000150.1:n.1244-121_1244-115delinsTTCACCA
NM_001105578.2:c.645_651delinsTGGTGAA (SYCE2) MANE Select	NP_001099048.1:p.Asp215=
NM_013976.4:c.1244-353_1244-347delinsTTCACCA (GCDH)	NP_039663.1:n.1244-353_1244-347delinsTTCACCA
NM_013976.5:c.1244-353_1244-347delinsTTCACCA (GCDH)	NP_039663.1:n.1244-353_1244-347delinsTTCACCA