Canonical Allele Identifier: CA2666706713
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585765_98585766insCACCATCCTGACA , CM000665.2:g.98585765_98585766insCACCATCCTGACA GRCh38
NC_000003.11:g.98304609_98304610insCACCATCCTGACA , CM000665.1:g.98304609_98304610insCACCATCCTGACA GRCh37
NC_000003.10:g.99787299_99787300insCACCATCCTGACA NCBI36
NG_015994.1:g.12847_12848insGTCAGGATGGTGT
NG_015994.2:g.12847_12848insGTCAGGATGGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-106_954-105insGTCAGGATGGTGT MANE Select ENSP00000497326.1:n.954-106_954-105insGTCAGGATGGTGT
ENST00000264193.2:c.954-106_954-105insGTCAGGATGGTGT ENSP00000264193.2:n.954-106_954-105insGTCAGGATGGTGT
ENST00000510489.1:n.98_99insGTCAGGATGGTGT
NM_000097.5:c.954-106_954-105insGTCAGGATGGTGT NP_000088.3:n.954-106_954-105insGTCAGGATGGTGT
XM_005247125.3:c.954-106_954-105insGTCAGGATGGTGT XP_005247182.1:n.954-106_954-105insGTCAGGATGGTGT
NM_000097.7:c.954-106_954-105insGTCAGGATGGTGT MANE Select NP_000088.3:n.954-106_954-105insGTCAGGATGGTGT
XM_005247125.4:c.954-106_954-105insGTCAGGATGGTGT XP_005247182.1:n.954-106_954-105insGTCAGGATGGTGT
XR_001740025.2:n.1125-106_1125-105insGTCAGGATGGTGT
XR_001740026.1:n.1583_1584insGTCAGGATGGTGT
XR_001740027.1:n.1229-106_1229-105insGTCAGGATGGTGT
XR_001740028.1:n.1195-106_1195-105insGTCAGGATGGTGT