Canonical Allele Identifier: CA404315727

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12892119T>G , CM000681.2:g.12892119T>G	GRCh38
NC_000019.9:g.13002933T>G , CM000681.1:g.13002933T>G	GRCh37
NC_000019.8:g.12863933T>G	NCBI36
NG_009292.1:g.5960T>G
NG_013087.1:g.85A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000159.4:c.275T>G MANE Select	NP_000150.1:p.Phe92Cys
ENST00000222214.10:c.275T>G MANE Select	ENSP00000222214.4:p.Phe92Cys
NM_000159.3:c.275T>G	NP_000150.1:p.Phe92Cys
NM_013976.3:c.275T>G	NP_039663.1:p.Phe92Cys
NM_013976.4:c.275T>G	NP_039663.1:p.Phe92Cys
NM_013976.5:c.275T>G	NP_039663.1:p.Phe92Cys
NR_102316.1:n.379+145T>G
NR_102317.1:n.691T>G
ENST00000222214.9:c.275T>G	ENSP00000222214.4:p.Phe92Cys
ENST00000421816.6:n.312+145T>G
ENST00000585420.5:n.640T>G
ENST00000585760.5:n.311T>G
ENST00000587072.1:c.275T>G	ENSP00000468584.1:p.Phe92Cys
ENST00000587832.5:n.332T>G
ENST00000588905.5:c.239T>G	ENSP00000465770.1:p.Phe80Cys
ENST00000589039.5:c.271+145T>G	ENSP00000465618.1:n.271+145T>G
ENST00000590445.5:c.*152T>G	ENSP00000468125.1:n.*152T>G
ENST00000590530.5:c.271+145T>G	ENSP00000468452.1:n.271+145T>G
ENST00000590627.5:n.640T>G
ENST00000591043.1:n.311T>G
ENST00000591470.5:c.275T>G	ENSP00000466845.1:p.Phe92Cys
XM_006722721.2:c.275T>G	XP_006722784.1:p.Phe92Cys
XM_011527899.1:c.275T>G	XP_011526201.1:p.Phe92Cys
XM_011527899.2:c.275T>G	XP_011526201.1:p.Phe92Cys
XM_011527900.1:c.275T>G	XP_011526202.1:p.Phe92Cys
XM_011527900.2:c.275T>G	XP_011526202.1:p.Phe92Cys
XM_017026580.1:c.275T>G	XP_016882069.1:p.Phe92Cys