Canonical Allele Identifier: CA2756307267

Gene: CHDH

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53844912del , CM000665.2:g.53844912del	GRCh38
NC_000003.11:g.53878939del , CM000665.1:g.53878939del	GRCh37
NC_000003.10:g.53853979del	NCBI36
NG_028042.1:g.6484del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315251.11:c.-131+1173del MANE Select	ENSP00000319851.5:n.-131+1173del
ENST00000315251.10:c.-131+1173del	ENSP00000319851.5:n.-131+1173del
NM_018397.4:c.-131+1173del	NP_060867.2:n.-131+1173del
XM_006713250.2:c.-131+1173del	XP_006713313.1:n.-131+1173del
XM_006713251.2:c.-131+912del	XP_006713314.1:n.-131+912del
XM_006713252.2:c.-131+1173del	XP_006713315.1:n.-131+1173del
XM_011533939.1:c.-198del	XP_011532241.1:n.-198del
XM_006713250.4:c.-131+1173del	XP_006713313.1:n.-131+1173del
XM_006713251.4:c.-131+912del	XP_006713314.1:n.-131+912del
XM_006713252.4:c.-131+1173del	XP_006713315.1:n.-131+1173del
XM_011533939.3:c.-198del	XP_011532241.1:n.-198del
XM_017006799.2:c.-131+1173del	XP_016862288.1:n.-131+1173del
XR_001740199.2:n.382+1173del
XR_002959545.1:n.382+1173del
NM_018397.5:c.-131+1173del MANE Select	NP_060867.2:n.-131+1173del