Canonical Allele Identifier: CA2666706646

Gene: CPOX

Linked Data

• gnomAD v4: 3-98585418-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585418G>T , CM000665.2:g.98585418G>T	GRCh38
NC_000003.11:g.98304262G>T , CM000665.1:g.98304262G>T	GRCh37
NC_000003.10:g.99786952G>T	NCBI36
NG_015994.1:g.13194C>A
NG_015994.2:g.13194C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.58+23C>A
ENST00000647941.2:c.1172+23C>A MANE Select	ENSP00000497326.1:n.1172+23C>A
ENST00000264193.2:c.1172+23C>A	ENSP00000264193.2:n.1172+23C>A
ENST00000510489.1:n.422+23C>A
ENST00000512905.5:c.58+23C>A
NM_000097.5:c.1172+23C>A	NP_000088.3:n.1172+23C>A
XM_005247125.3:c.1172+23C>A	XP_005247182.1:n.1172+23C>A
NM_000097.7:c.1172+23C>A MANE Select	NP_000088.3:n.1172+23C>A
XM_005247125.4:c.1172+23C>A	XP_005247182.1:n.1172+23C>A
XR_001740025.2:n.1343+23C>A
XR_001740026.1:n.1907+23C>A
XR_001740027.1:n.1447+23C>A
XR_001740028.1:n.1413+23C>A