Canonical Allele Identifier: CA1051334557

Gene: CPOX

Linked Data

• gnomAD v3: 3-98585598-A-ATTTTTT
• gnomAD v4: 3-98585598-A-ATTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585598_98585599insTTTTTT , CM000665.2:g.98585598_98585599insTTTTTT	GRCh38
NC_000003.11:g.98304442_98304443insTTTTTT , CM000665.1:g.98304442_98304443insTTTTTT	GRCh37
NC_000003.10:g.99787132_99787133insTTTTTT	NCBI36
NG_015994.1:g.13013_13014insAAAAAA
NG_015994.2:g.13013_13014insAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.1014_1015insAAAAAA MANE Select	ENSP00000497326.1:p.Phe338_Phe339insLysLys
ENST00000264193.2:c.1014_1015insAAAAAA	ENSP00000264193.2:p.Phe338_Phe339insLysLys
ENST00000510489.1:n.264_265insAAAAAA
NM_000097.5:c.1014_1015insAAAAAA	NP_000088.3:p.Phe338_Phe339insLysLys
XM_005247125.3:c.1014_1015insAAAAAA	XP_005247182.1:p.Phe338_Phe339insLysLys
NM_000097.7:c.1014_1015insAAAAAA MANE Select	NP_000088.3:p.Phe338_Phe339insLysLys
XM_005247125.4:c.1014_1015insAAAAAA	XP_005247182.1:p.Phe338_Phe339insLysLys
XR_001740025.2:n.1185_1186insAAAAAA
XR_001740026.1:n.1749_1750insAAAAAA
XR_001740027.1:n.1289_1290insAAAAAA
XR_001740028.1:n.1255_1256insAAAAAA