Canonical Allele Identifier: CA305500974

Gene: GCDH SYCE2

Linked Data

• dbSNP Id: rs993539907
• MyVariant Identifiers: chr19:g.13010137T>C (hg19) ; chr19:g.12899323T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12899323T>C , CM000681.2:g.12899323T>C	GRCh38
NC_000019.9:g.13010137T>C , CM000681.1:g.13010137T>C	GRCh37
NC_000019.8:g.12871137T>C	NCBI36
NG_009292.1:g.13164T>C
NG_033049.1:g.24950A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1244-145T>C (GCDH) MANE Select	ENSP00000222214.4:n.1244-145T>C
ENST00000293695.8:c.*18A>G (SYCE2) MANE Select	ENSP00000293695.6:n.*18A>G
ENST00000222214.9:c.1244-145T>C (GCDH)	ENSP00000222214.4:n.1244-145T>C
ENST00000293695.7:c.*18A>G (SYCE2)	ENSP00000293695.6:n.*18A>G
ENST00000585420.5:n.1574-145T>C (GCDH)
ENST00000590530.5:c.*684-145T>C (GCDH)	ENSP00000468452.1:n.*684-145T>C
ENST00000591043.1:n.1554-145T>C (GCDH)
ENST00000591050.1:c.210+1460T>C (GCDH)
ENST00000591470.5:c.1244-145T>C (GCDH)	ENSP00000466845.1:n.1244-145T>C
ENST00000592819.1:c.248A>G (SYCE2)
NM_000159.3:c.1244-145T>C (GCDH)	NP_000150.1:n.1244-145T>C
NM_001105578.1:c.*18A>G (SYCE2)	NP_001099048.1:n.*18A>G
NM_013976.3:c.1244-377T>C (GCDH)	NP_039663.1:n.1244-377T>C
NR_102316.1:n.1407-145T>C (GCDH)
NR_102317.1:n.1625-145T>C (GCDH)
XM_005259848.3:c.*85A>G (SYCE2)	XP_005259905.1:n.*85A>G
XM_006722721.2:c.1244-911T>C (GCDH)	XP_006722784.1:n.1244-911T>C
XM_011527882.1:c.*18A>G (SYCE2)	XP_011526184.1:n.*18A>G
XM_011527883.1:c.*85A>G (SYCE2)	XP_011526185.1:n.*85A>G
XM_011527899.1:c.1243+1460T>C (GCDH)	XP_011526201.1:n.1243+1460T>C
XM_011527900.1:c.1244-911T>C (GCDH)	XP_011526202.1:n.1244-911T>C
XM_005259848.4:c.*85A>G (SYCE2)	XP_005259905.1:n.*85A>G
XM_011527882.2:c.*18A>G (SYCE2)	XP_011526184.1:n.*18A>G
XM_011527883.2:c.*85A>G (SYCE2)	XP_011526185.1:n.*85A>G
XM_011527899.2:c.1243+1460T>C (GCDH)	XP_011526201.1:n.1243+1460T>C
XM_011527900.2:c.1244-911T>C (GCDH)	XP_011526202.1:n.1244-911T>C
XM_017026580.1:c.1244-911T>C (GCDH)	XP_016882069.1:n.1244-911T>C
NM_000159.4:c.1244-145T>C (GCDH) MANE Select	NP_000150.1:n.1244-145T>C
NM_001105578.2:c.*18A>G (SYCE2) MANE Select	NP_001099048.1:n.*18A>G
NM_013976.4:c.1244-377T>C (GCDH)	NP_039663.1:n.1244-377T>C
NM_013976.5:c.1244-377T>C (GCDH)	NP_039663.1:n.1244-377T>C