Canonical Allele Identifier: CA2666706682

Gene: CPOX

Linked Data

• gnomAD v4: 3-98585714-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585715_98585716insTA , CM000665.2:g.98585715_98585716insTA	GRCh38
NC_000003.11:g.98304559_98304560insTA , CM000665.1:g.98304559_98304560insTA	GRCh37
NC_000003.10:g.99787249_99787250insTA	NCBI36
NG_015994.1:g.12897_12898insAT
NG_015994.2:g.12897_12898insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.954-56_954-55insAT MANE Select	ENSP00000497326.1:n.954-56_954-55insAT
ENST00000264193.2:c.954-56_954-55insAT	ENSP00000264193.2:n.954-56_954-55insAT
ENST00000510489.1:n.148_149insAT
NM_000097.5:c.954-56_954-55insAT	NP_000088.3:n.954-56_954-55insAT
XM_005247125.3:c.954-56_954-55insAT	XP_005247182.1:n.954-56_954-55insAT
NM_000097.7:c.954-56_954-55insAT MANE Select	NP_000088.3:n.954-56_954-55insAT
XM_005247125.4:c.954-56_954-55insAT	XP_005247182.1:n.954-56_954-55insAT
XR_001740025.2:n.1125-56_1125-55insAT
XR_001740026.1:n.1633_1634insAT
XR_001740027.1:n.1229-56_1229-55insAT
XR_001740028.1:n.1195-56_1195-55insAT