Canonical Allele Identifier: CA2666148312
Gene: CHDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53844730_53844737del , CM000665.2:g.53844730_53844737del GRCh38
NC_000003.11:g.53878757_53878764del , CM000665.1:g.53878757_53878764del GRCh37
NC_000003.10:g.53853797_53853804del NCBI36
NG_028042.1:g.6657_6664del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315251.11:c.-131+1346_-131+1353del MANE Select ENSP00000319851.5:n.-131+1346_-131+1353del
ENST00000315251.10:c.-131+1346_-131+1353del ENSP00000319851.5:n.-131+1346_-131+1353del
ENST00000467802.1:c.-155_-148del ENSP00000419863.1:n.-155_-148del
NM_018397.4:c.-131+1346_-131+1353del NP_060867.2:n.-131+1346_-131+1353del
XM_006713250.2:c.-131+1346_-131+1353del XP_006713313.1:n.-131+1346_-131+1353del
XM_006713251.2:c.-131+1085_-131+1092del XP_006713314.1:n.-131+1085_-131+1092del
XM_006713252.2:c.-131+1346_-131+1353del XP_006713315.1:n.-131+1346_-131+1353del
XM_011533938.1:c.-155_-148del XP_011532240.1:n.-155_-148del
XM_011533939.1:c.-131+106_-131+113del XP_011532241.1:n.-131+106_-131+113del
XM_006713250.4:c.-131+1346_-131+1353del XP_006713313.1:n.-131+1346_-131+1353del
XM_006713251.4:c.-131+1085_-131+1092del XP_006713314.1:n.-131+1085_-131+1092del
XM_006713252.4:c.-131+1346_-131+1353del XP_006713315.1:n.-131+1346_-131+1353del
XM_011533938.3:c.-155_-148del XP_011532240.1:n.-155_-148del
XM_011533939.3:c.-131+106_-131+113del XP_011532241.1:n.-131+106_-131+113del
XM_017006797.2:c.-155_-148del XP_016862286.1:n.-155_-148del
XM_017006799.2:c.-131+1346_-131+1353del XP_016862288.1:n.-131+1346_-131+1353del
XR_001740199.2:n.382+1346_382+1353del
XR_002959545.1:n.382+1346_382+1353del
NM_018397.5:c.-131+1346_-131+1353del MANE Select NP_060867.2:n.-131+1346_-131+1353del