Canonical Allele Identifier: CA1387393478

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585437T= , CM000665.2:g.98585437T=	GRCh38
NC_000003.11:g.98304281T= , CM000665.1:g.98304281T=	GRCh37
NC_000003.10:g.99786971T=	NCBI36
NG_015994.1:g.13175A=
NG_015994.2:g.13175A=

Transcript Alleles

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