Canonical Allele Identifier: CA2666706681

Gene: CPOX

Linked Data

• gnomAD v4: 3-98585712-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585716dup , CM000665.2:g.98585716dup	GRCh38
NC_000003.11:g.98304560dup , CM000665.1:g.98304560dup	GRCh37
NC_000003.10:g.99787250dup	NCBI36
NG_015994.1:g.12899dup
NG_015994.2:g.12899dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.954-54dup MANE Select	ENSP00000497326.1:n.954-54dup
ENST00000264193.2:c.954-54dup	ENSP00000264193.2:n.954-54dup
ENST00000510489.1:n.150dup
NM_000097.5:c.954-54dup	NP_000088.3:n.954-54dup
XM_005247125.3:c.954-54dup	XP_005247182.1:n.954-54dup
NM_000097.7:c.954-54dup MANE Select	NP_000088.3:n.954-54dup
XM_005247125.4:c.954-54dup	XP_005247182.1:n.954-54dup
XR_001740025.2:n.1125-54dup
XR_001740026.1:n.1635dup
XR_001740027.1:n.1229-54dup
XR_001740028.1:n.1195-54dup