Canonical Allele Identifier: CA2577832751

Gene: CPOX

Linked Data

• gnomAD v4: 3-98585429-CCAGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585432_98585435del , CM000665.2:g.98585432_98585435del	GRCh38
NC_000003.11:g.98304276_98304279del , CM000665.1:g.98304276_98304279del	GRCh37
NC_000003.10:g.99786966_99786969del	NCBI36
NG_015994.1:g.13179_13182del
NG_015994.2:g.13179_13182del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.58+8_58+11del
ENST00000647941.2:c.1172+8_1172+11del MANE Select	ENSP00000497326.1:n.1172+8_1172+11del
ENST00000264193.2:c.1172+8_1172+11del	ENSP00000264193.2:n.1172+8_1172+11del
ENST00000510489.1:n.422+8_422+11del
ENST00000512905.5:c.58+8_58+11del
NM_000097.5:c.1172+8_1172+11del	NP_000088.3:n.1172+8_1172+11del
XM_005247125.3:c.1172+8_1172+11del	XP_005247182.1:n.1172+8_1172+11del
NM_000097.7:c.1172+8_1172+11del MANE Select	NP_000088.3:n.1172+8_1172+11del
XM_005247125.4:c.1172+8_1172+11del	XP_005247182.1:n.1172+8_1172+11del
XR_001740025.2:n.1343+8_1343+11del
XR_001740026.1:n.1907+8_1907+11del
XR_001740027.1:n.1447+8_1447+11del
XR_001740028.1:n.1413+8_1413+11del