Canonical Allele Identifier: CA2666706599

Gene: CPOX

Linked Data

• gnomAD v4: 3-98585338-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585339dup , CM000665.2:g.98585339dup	GRCh38
NC_000003.11:g.98304183dup , CM000665.1:g.98304183dup	GRCh37
NC_000003.10:g.99786873dup	NCBI36
NG_015994.1:g.13273dup
NG_015994.2:g.13273dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.58+102dup
ENST00000647941.2:c.1172+102dup MANE Select	ENSP00000497326.1:n.1172+102dup
ENST00000264193.2:c.1172+102dup	ENSP00000264193.2:n.1172+102dup
ENST00000510489.1:n.422+102dup
ENST00000512905.5:c.58+102dup
NM_000097.5:c.1172+102dup	NP_000088.3:n.1172+102dup
XM_005247125.3:c.1172+102dup	XP_005247182.1:n.1172+102dup
NM_000097.7:c.1172+102dup MANE Select	NP_000088.3:n.1172+102dup
XM_005247125.4:c.1172+102dup	XP_005247182.1:n.1172+102dup
XR_001740025.2:n.1343+102dup
XR_001740026.1:n.1907+102dup
XR_001740027.1:n.1447+102dup
XR_001740028.1:n.1413+102dup