Canonical Allele Identifier: CA353645878

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98590743C>T , CM000665.2:g.98590743C>T	GRCh38
NC_000003.11:g.98309587C>T , CM000665.1:g.98309587C>T	GRCh37
NC_000003.10:g.99792277C>T	NCBI36
NG_015994.1:g.7869G>A
NG_015994.2:g.7869G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.701-1G>A MANE Select	ENSP00000497326.1:n.701-1G>A
ENST00000264193.2:c.701-1G>A	ENSP00000264193.2:n.701-1G>A
ENST00000513674.1:c.*34-86G>A	ENSP00000424924.1:n.*34-86G>A
ENST00000515041.1:n.807-1G>A
NM_000097.5:c.701-1G>A	NP_000088.3:n.701-1G>A
XM_005247125.3:c.701-1G>A	XP_005247182.1:n.701-1G>A
XM_011512437.1:c.701-1G>A	XP_011510739.1:n.701-1G>A
NM_000097.7:c.701-1G>A MANE Select	NP_000088.3:n.701-1G>A
XM_005247125.4:c.701-1G>A	XP_005247182.1:n.701-1G>A
XR_001740025.2:n.872-1G>A
XR_001740026.1:n.877-1G>A
XR_001740027.1:n.881-1G>A
XR_001740028.1:n.881-1G>A