Canonical Allele Identifier: CA1387393821
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585697_98585698delinsGA , CM000665.2:g.98585697_98585698delinsGA GRCh38
NC_000003.11:g.98304541_98304542delinsGA , CM000665.1:g.98304541_98304542delinsGA GRCh37
NC_000003.10:g.99787231_99787232delinsGA NCBI36
NG_015994.1:g.12914_12915delinsTC
NG_015994.2:g.12914_12915delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-39_954-38delinsTC MANE Select ENSP00000497326.1:n.954-39_954-38delinsTC
ENST00000264193.2:c.954-39_954-38delinsTC ENSP00000264193.2:n.954-39_954-38delinsTC
ENST00000510489.1:n.165_166delinsTC
NM_000097.5:c.954-39_954-38delinsTC NP_000088.3:n.954-39_954-38delinsTC
XM_005247125.3:c.954-39_954-38delinsTC XP_005247182.1:n.954-39_954-38delinsTC
NM_000097.7:c.954-39_954-38delinsTC MANE Select NP_000088.3:n.954-39_954-38delinsTC
XM_005247125.4:c.954-39_954-38delinsTC XP_005247182.1:n.954-39_954-38delinsTC
XR_001740025.2:n.1125-39_1125-38delinsTC
XR_001740026.1:n.1650_1651delinsTC
XR_001740027.1:n.1229-39_1229-38delinsTC
XR_001740028.1:n.1195-39_1195-38delinsTC