Canonical Allele Identifier: CA1387393372

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585315_98585316delinsAT , CM000665.2:g.98585315_98585316delinsAT	GRCh38
NC_000003.11:g.98304159_98304160delinsAT , CM000665.1:g.98304159_98304160delinsAT	GRCh37
NC_000003.10:g.99786849_99786850delinsAT	NCBI36
NG_015994.1:g.13296_13297delinsAT
NG_015994.2:g.13296_13297delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.58+125_58+126delinsAT
ENST00000647941.2:c.1172+125_1172+126delinsAT MANE Select	ENSP00000497326.1:n.1172+125_1172+126delinsAT
ENST00000264193.2:c.1172+125_1172+126delinsAT	ENSP00000264193.2:n.1172+125_1172+126delinsAT
ENST00000510489.1:n.422+125_422+126delinsAT
ENST00000512905.5:c.58+125_58+126delinsAT
NM_000097.5:c.1172+125_1172+126delinsAT	NP_000088.3:n.1172+125_1172+126delinsAT
XM_005247125.3:c.1172+125_1172+126delinsAT	XP_005247182.1:n.1172+125_1172+126delinsAT
NM_000097.7:c.1172+125_1172+126delinsAT MANE Select	NP_000088.3:n.1172+125_1172+126delinsAT
XM_005247125.4:c.1172+125_1172+126delinsAT	XP_005247182.1:n.1172+125_1172+126delinsAT
XR_001740025.2:n.1343+125_1343+126delinsAT
XR_001740026.1:n.1907+125_1907+126delinsAT
XR_001740027.1:n.1447+125_1447+126delinsAT
XR_001740028.1:n.1413+125_1413+126delinsAT