Canonical Allele Identifier: CA2323625052

Gene: GCDH SYCE2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12899747G= , CM000681.2:g.12899747G=	GRCh38
NC_000019.9:g.13010561G= , CM000681.1:g.13010561G=	GRCh37
NC_000019.8:g.12871561G=	NCBI36
NG_009292.1:g.13588G=
NG_033049.1:g.24526C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.*206G= (GCDH) MANE Select	ENSP00000222214.4:n.*206G=
ENST00000293695.8:c.612+257C= (SYCE2) MANE Select	ENSP00000293695.6:n.612+257C=
ENST00000222214.9:c.*206G= (GCDH)	ENSP00000222214.4:n.*206G=
ENST00000293695.7:c.612+257C= (SYCE2)	ENSP00000293695.6:n.612+257C=
ENST00000588242.2:n.177G= (GCDH)
ENST00000590530.5:c.*963G= (GCDH)	ENSP00000468452.1:n.*963G=
ENST00000591050.1:c.210+1884G= (GCDH)
ENST00000591470.5:c.*206G= (GCDH)	ENSP00000466845.1:n.*206G=
ENST00000592819.1:c.185+211C= (SYCE2)
NM_000159.3:c.*206G= (GCDH)	NP_000150.1:n.*206G=
NM_001105578.1:c.612+257C= (SYCE2)	NP_001099048.1:n.612+257C=
NM_013976.3:c.*4G= (GCDH)	NP_039663.1:n.*4G=
NR_102316.1:n.1686G= (GCDH)
NR_102317.1:n.1904G= (GCDH)
XM_005259848.3:c.*22+211C= (SYCE2)	XP_005259905.1:n.*22+211C=
XM_006722721.2:c.1244-487G= (GCDH)	XP_006722784.1:n.1244-487G=
XM_011527882.1:c.609+257C= (SYCE2)	XP_011526184.1:n.609+257C=
XM_011527883.1:c.*22+211C= (SYCE2)	XP_011526185.1:n.*22+211C=
XM_011527899.1:c.1243+1884G= (GCDH)	XP_011526201.1:n.1243+1884G=
XM_011527900.1:c.1244-487G= (GCDH)	XP_011526202.1:n.1244-487G=
XM_005259848.4:c.*22+211C= (SYCE2)	XP_005259905.1:n.*22+211C=
XM_011527882.2:c.609+257C= (SYCE2)	XP_011526184.1:n.609+257C=
XM_011527883.2:c.*22+211C= (SYCE2)	XP_011526185.1:n.*22+211C=
XM_011527899.2:c.1243+1884G= (GCDH)	XP_011526201.1:n.1243+1884G=
XM_011527900.2:c.1244-487G= (GCDH)	XP_011526202.1:n.1244-487G=
XM_017026580.1:c.1244-487G= (GCDH)	XP_016882069.1:n.1244-487G=
NM_000159.4:c.*206G= (GCDH) MANE Select	NP_000150.1:n.*206G=
NM_001105578.2:c.612+257C= (SYCE2) MANE Select	NP_001099048.1:n.612+257C=
NM_013976.4:c.*4G= (GCDH)	NP_039663.1:n.*4G=
NM_013976.5:c.*4G= (GCDH)	NP_039663.1:n.*4G=