Canonical Allele Identifier: CA404322031

Gene: GCDH SYCE2

Linked Data

• MyVariant Identifiers: chr19:g.13010177G>T (hg19) ; chr19:g.12899363G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12899363G>T , CM000681.2:g.12899363G>T	GRCh38
NC_000019.9:g.13010177G>T , CM000681.1:g.13010177G>T	GRCh37
NC_000019.8:g.12871177G>T	NCBI36
NG_009292.1:g.13204G>T
NG_033049.1:g.24910C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1244-105G>T (GCDH) MANE Select	ENSP00000222214.4:n.1244-105G>T
ENST00000293695.8:c.635C>A (SYCE2) MANE Select	ENSP00000293695.6:p.Thr212Asn
ENST00000222214.9:c.1244-105G>T (GCDH)	ENSP00000222214.4:n.1244-105G>T
ENST00000293695.7:c.635C>A (SYCE2)	ENSP00000293695.6:p.Thr212Asn
ENST00000585420.5:n.1574-105G>T (GCDH)
ENST00000590530.5:c.*684-105G>T (GCDH)	ENSP00000468452.1:n.*684-105G>T
ENST00000591043.1:n.1554-105G>T (GCDH)
ENST00000591050.1:c.210+1500G>T (GCDH)
ENST00000591470.5:c.1244-105G>T (GCDH)	ENSP00000466845.1:n.1244-105G>T
ENST00000592819.1:c.208C>A (SYCE2)
NM_000159.3:c.1244-105G>T (GCDH)	NP_000150.1:n.1244-105G>T
NM_001105578.1:c.635C>A (SYCE2)	NP_001099048.1:p.Thr212Asn
NM_013976.3:c.1244-337G>T (GCDH)	NP_039663.1:n.1244-337G>T
NR_102316.1:n.1407-105G>T (GCDH)
NR_102317.1:n.1625-105G>T (GCDH)
XM_005259848.3:c.*45C>A (SYCE2)	XP_005259905.1:n.*45C>A
XM_006722721.2:c.1244-871G>T (GCDH)	XP_006722784.1:n.1244-871G>T
XM_011527882.1:c.632C>A (SYCE2)	XP_011526184.1:p.Thr211Asn
XM_011527883.1:c.*45C>A (SYCE2)	XP_011526185.1:n.*45C>A
XM_011527899.1:c.1243+1500G>T (GCDH)	XP_011526201.1:n.1243+1500G>T
XM_011527900.1:c.1244-871G>T (GCDH)	XP_011526202.1:n.1244-871G>T
XM_005259848.4:c.*45C>A (SYCE2)	XP_005259905.1:n.*45C>A
XM_011527882.2:c.632C>A (SYCE2)	XP_011526184.1:p.Thr211Asn
XM_011527883.2:c.*45C>A (SYCE2)	XP_011526185.1:n.*45C>A
XM_011527899.2:c.1243+1500G>T (GCDH)	XP_011526201.1:n.1243+1500G>T
XM_011527900.2:c.1244-871G>T (GCDH)	XP_011526202.1:n.1244-871G>T
XM_017026580.1:c.1244-871G>T (GCDH)	XP_016882069.1:n.1244-871G>T
NM_000159.4:c.1244-105G>T (GCDH) MANE Select	NP_000150.1:n.1244-105G>T
NM_001105578.2:c.635C>A (SYCE2) MANE Select	NP_001099048.1:p.Thr212Asn
NM_013976.4:c.1244-337G>T (GCDH)	NP_039663.1:n.1244-337G>T
NM_013976.5:c.1244-337G>T (GCDH)	NP_039663.1:n.1244-337G>T