Canonical Allele Identifier: CA2323620856

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891387C= , CM000681.2:g.12891387C=	GRCh38
NC_000019.9:g.13002201C= , CM000681.1:g.13002201C=	GRCh37
NC_000019.8:g.12863201C=	NCBI36
NG_009292.1:g.5228C=
NG_013087.1:g.817G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.83C= MANE Select	ENSP00000222214.4:p.Ala28=
ENST00000222214.9:c.83C=	ENSP00000222214.4:p.Ala28=
ENST00000421816.6:n.160C=
ENST00000585420.5:n.140C=
ENST00000585760.5:n.119C=
ENST00000587072.1:c.83C=	ENSP00000468584.1:p.Ala28=
ENST00000587832.5:n.140C=
ENST00000588905.5:c.83C=	ENSP00000465770.1:p.Ala28=
ENST00000589039.5:c.83C=	ENSP00000465618.1:p.Ala28=
ENST00000590445.5:c.83C=	ENSP00000468125.1:p.Ala28=
ENST00000590530.5:c.83C=	ENSP00000468452.1:p.Ala28=
ENST00000590627.5:n.140C=
ENST00000591043.1:n.119C=
ENST00000591470.5:c.83C=	ENSP00000466845.1:p.Ala28=
NM_000159.3:c.83C=	NP_000150.1:p.Ala28=
NM_013976.3:c.83C=	NP_039663.1:p.Ala28=
NR_102316.1:n.191C=
NR_102317.1:n.191C=
XM_006722721.2:c.83C=	XP_006722784.1:p.Ala28=
XM_011527899.1:c.83C=	XP_011526201.1:p.Ala28=
XM_011527900.1:c.83C=	XP_011526202.1:p.Ala28=
XM_011527899.2:c.83C=	XP_011526201.1:p.Ala28=
XM_011527900.2:c.83C=	XP_011526202.1:p.Ala28=
XM_017026580.1:c.83C=	XP_016882069.1:p.Ala28=
NM_000159.4:c.83C= MANE Select	NP_000150.1:p.Ala28=
NM_013976.4:c.83C=	NP_039663.1:p.Ala28=
NM_013976.5:c.83C=	NP_039663.1:p.Ala28=