Canonical Allele Identifier: CA2576639019

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891297G>C , CM000681.2:g.12891297G>C	GRCh38
NC_000019.9:g.13002111G>C , CM000681.1:g.13002111G>C	GRCh37
NC_000019.8:g.12863111G>C	NCBI36
NG_009292.1:g.5138G>C
NG_013087.1:g.907C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.-8G>C MANE Select	ENSP00000222214.4:n.-8G>C
ENST00000222214.9:c.-8G>C	ENSP00000222214.4:n.-8G>C
ENST00000421816.6:n.70G>C
ENST00000585420.5:n.50G>C
ENST00000585760.5:n.29G>C
ENST00000587072.1:c.-8G>C	ENSP00000468584.1:n.-8G>C
ENST00000587832.5:n.50G>C
ENST00000588905.5:c.-8G>C	ENSP00000465770.1:n.-8G>C
ENST00000589039.5:c.-8G>C	ENSP00000465618.1:n.-8G>C
ENST00000590445.5:c.-8G>C	ENSP00000468125.1:n.-8G>C
ENST00000590530.5:c.-8G>C	ENSP00000468452.1:n.-8G>C
ENST00000590627.5:n.50G>C
ENST00000591043.1:n.29G>C
ENST00000591470.5:c.-8G>C	ENSP00000466845.1:n.-8G>C
NM_000159.3:c.-8G>C	NP_000150.1:n.-8G>C
NM_013976.3:c.-8G>C	NP_039663.1:n.-8G>C
NR_102316.1:n.101G>C
NR_102317.1:n.101G>C
XM_006722721.2:c.-8G>C	XP_006722784.1:n.-8G>C
XM_011527899.1:c.-8G>C	XP_011526201.1:n.-8G>C
XM_011527900.1:c.-8G>C	XP_011526202.1:n.-8G>C
XM_011527899.2:c.-8G>C	XP_011526201.1:n.-8G>C
XM_011527900.2:c.-8G>C	XP_011526202.1:n.-8G>C
XM_017026580.1:c.-8G>C	XP_016882069.1:n.-8G>C
NM_000159.4:c.-8G>C MANE Select	NP_000150.1:n.-8G>C
NM_013976.4:c.-8G>C	NP_039663.1:n.-8G>C
NM_013976.5:c.-8G>C	NP_039663.1:n.-8G>C