Canonical Allele Identifier: CA783396304

Gene: GCDH

Linked Data

• dbSNP Id: rs1326996633
• MyVariant Identifiers: chr19:g.13002459C>G (hg19) ; chr19:g.12891645C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891645C>G , CM000681.2:g.12891645C>G	GRCh38
NC_000019.9:g.13002459C>G , CM000681.1:g.13002459C>G	GRCh37
NC_000019.8:g.12863459C>G	NCBI36
NG_009292.1:g.5486C>G
NG_013087.1:g.559G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.127+123C>G MANE Select	ENSP00000222214.4:n.127+123C>G
ENST00000222214.9:c.127+123C>G	ENSP00000222214.4:n.127+123C>G
ENST00000421816.6:n.169-186C>G
ENST00000585420.5:n.307C>G
ENST00000585760.5:n.163+123C>G
ENST00000587072.1:c.127+123C>G	ENSP00000468584.1:n.127+123C>G
ENST00000587832.5:n.184+123C>G
ENST00000588905.5:c.92-186C>G	ENSP00000465770.1:n.92-186C>G
ENST00000589039.5:c.127+123C>G	ENSP00000465618.1:n.127+123C>G
ENST00000590445.5:c.250C>G	ENSP00000468125.1:p.Gln84Glu
ENST00000590530.5:c.127+123C>G	ENSP00000468452.1:n.127+123C>G
ENST00000590627.5:n.307C>G
ENST00000591043.1:n.163+123C>G
ENST00000591470.5:c.127+123C>G	ENSP00000466845.1:n.127+123C>G
NM_000159.3:c.127+123C>G	NP_000150.1:n.127+123C>G
NM_013976.3:c.127+123C>G	NP_039663.1:n.127+123C>G
NR_102316.1:n.235+123C>G
NR_102317.1:n.358C>G
XM_006722721.2:c.127+123C>G	XP_006722784.1:n.127+123C>G
XM_011527899.1:c.127+123C>G	XP_011526201.1:n.127+123C>G
XM_011527900.1:c.127+123C>G	XP_011526202.1:n.127+123C>G
XM_011527899.2:c.127+123C>G	XP_011526201.1:n.127+123C>G
XM_011527900.2:c.127+123C>G	XP_011526202.1:n.127+123C>G
XM_017026580.1:c.127+123C>G	XP_016882069.1:n.127+123C>G
NM_000159.4:c.127+123C>G MANE Select	NP_000150.1:n.127+123C>G
NM_013976.4:c.127+123C>G	NP_039663.1:n.127+123C>G
NM_013976.5:c.127+123C>G	NP_039663.1:n.127+123C>G