Canonical Allele Identifier: CA404315064

Gene: GCDH

Linked Data

• MyVariant Identifiers: chr19:g.13002708A>T (hg19) ; chr19:g.12891894A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891894A>T , CM000681.2:g.12891894A>T	GRCh38
NC_000019.9:g.13002708A>T , CM000681.1:g.13002708A>T	GRCh37
NC_000019.8:g.12863708A>T	NCBI36
NG_009292.1:g.5735A>T
NG_013087.1:g.310T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.191A>T MANE Select	ENSP00000222214.4:p.Glu64Val
ENST00000222214.9:c.191A>T	ENSP00000222214.4:p.Glu64Val
ENST00000421816.6:n.232A>T
ENST00000585420.5:n.556A>T
ENST00000585760.5:n.227A>T
ENST00000587072.1:c.191A>T	ENSP00000468584.1:p.Glu64Val
ENST00000587832.5:n.248A>T
ENST00000588905.5:c.155A>T	ENSP00000465770.1:p.Glu52Val
ENST00000589039.5:c.191A>T	ENSP00000465618.1:p.Glu64Val
ENST00000590445.5:c.*68A>T	ENSP00000468125.1:n.*68A>T
ENST00000590530.5:c.191A>T	ENSP00000468452.1:p.Glu64Val
ENST00000590627.5:n.556A>T
ENST00000591043.1:n.227A>T
ENST00000591470.5:c.191A>T	ENSP00000466845.1:p.Glu64Val
NM_000159.3:c.191A>T	NP_000150.1:p.Glu64Val
NM_013976.3:c.191A>T	NP_039663.1:p.Glu64Val
NR_102316.1:n.299A>T
NR_102317.1:n.607A>T
XM_006722721.2:c.191A>T	XP_006722784.1:p.Glu64Val
XM_011527899.1:c.191A>T	XP_011526201.1:p.Glu64Val
XM_011527900.1:c.191A>T	XP_011526202.1:p.Glu64Val
XM_011527899.2:c.191A>T	XP_011526201.1:p.Glu64Val
XM_011527900.2:c.191A>T	XP_011526202.1:p.Glu64Val
XM_017026580.1:c.191A>T	XP_016882069.1:p.Glu64Val
NM_000159.4:c.191A>T MANE Select	NP_000150.1:p.Glu64Val
NM_013976.4:c.191A>T	NP_039663.1:p.Glu64Val
NM_013976.5:c.191A>T	NP_039663.1:p.Glu64Val