Canonical Allele Identifier: CA1365492685

Gene: CHDH

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53822023C= , CM000665.2:g.53822023C=	GRCh38
NC_000003.11:g.53856050C= , CM000665.1:g.53856050C=	GRCh37
NC_000003.10:g.53831090C=	NCBI36
NG_028042.1:g.29371G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315251.11:c.856-247G= MANE Select	ENSP00000319851.5:n.856-247G=
ENST00000315251.10:c.856-247G=	ENSP00000319851.5:n.856-247G=
NM_018397.4:c.856-247G=	NP_060867.2:n.856-247G=
XM_006713250.2:c.859-247G=	XP_006713313.1:n.859-247G=
XM_006713251.2:c.859-247G=	XP_006713314.1:n.859-247G=
XM_006713252.2:c.859-247G=	XP_006713315.1:n.859-247G=
XM_011533938.1:c.859-247G=	XP_011532240.1:n.859-247G=
XM_011533939.1:c.859-247G=	XP_011532241.1:n.859-247G=
XM_006713250.4:c.859-247G=	XP_006713313.1:n.859-247G=
XM_006713251.4:c.859-247G=	XP_006713314.1:n.859-247G=
XM_006713252.4:c.859-247G=	XP_006713315.1:n.859-247G=
XM_011533938.3:c.859-247G=	XP_011532240.1:n.859-247G=
XM_011533939.3:c.859-247G=	XP_011532241.1:n.859-247G=
XM_017006797.2:c.856-247G=	XP_016862286.1:n.856-247G=
XM_017006798.2:c.856-247G=	XP_016862287.1:n.856-247G=
XM_017006799.2:c.856-247G=	XP_016862288.1:n.856-247G=
XR_001740199.2:n.1371-247G=
XR_002959545.1:n.1371-247G=
NM_018397.5:c.856-247G= MANE Select	NP_060867.2:n.856-247G=