Canonical Allele Identifier: CA404316740

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893485T>C , CM000681.2:g.12893485T>C	GRCh38
NC_000019.9:g.13004299T>C , CM000681.1:g.13004299T>C	GRCh37
NC_000019.8:g.12865299T>C	NCBI36
NG_009292.1:g.7326T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000159.4:c.337T>C MANE Select	NP_000150.1:p.Tyr113His
ENST00000222214.10:c.337T>C MANE Select	ENSP00000222214.4:p.Tyr113His
NM_000159.3:c.337T>C	NP_000150.1:p.Tyr113His
NM_013976.3:c.337T>C	NP_039663.1:p.Tyr113His
NM_013976.4:c.337T>C	NP_039663.1:p.Tyr113His
NM_013976.5:c.337T>C	NP_039663.1:p.Tyr113His
NR_102316.1:n.500T>C
NR_102317.1:n.753T>C
ENST00000222214.9:c.337T>C	ENSP00000222214.4:p.Tyr113His
ENST00000421816.6:n.315T>C
ENST00000585420.5:n.702T>C
ENST00000587072.1:c.385T>C	ENSP00000468584.1:p.Tyr129His
ENST00000587832.5:n.394T>C
ENST00000588905.5:c.301T>C	ENSP00000465770.1:p.Tyr101His
ENST00000589039.5:c.274T>C	ENSP00000465618.1:p.Tyr92His
ENST00000590530.5:c.392T>C	ENSP00000468452.1:p.Ile131Thr
ENST00000590627.5:n.702T>C
ENST00000591043.1:n.373T>C
ENST00000591470.5:c.337T>C	ENSP00000466845.1:p.Tyr113His
XM_006722721.2:c.337T>C	XP_006722784.1:p.Tyr113His
XM_011527899.1:c.337T>C	XP_011526201.1:p.Tyr113His
XM_011527899.2:c.337T>C	XP_011526201.1:p.Tyr113His
XM_011527900.1:c.337T>C	XP_011526202.1:p.Tyr113His
XM_011527900.2:c.337T>C	XP_011526202.1:p.Tyr113His
XM_017026580.1:c.337T>C	XP_016882069.1:p.Tyr113His