Canonical Allele Identifier: CA1387393426

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585390G= , CM000665.2:g.98585390G=	GRCh38
NC_000003.11:g.98304234G= , CM000665.1:g.98304234G=	GRCh37
NC_000003.10:g.99786924G=	NCBI36
NG_015994.1:g.13222C=
NG_015994.2:g.13222C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.58+51C=
ENST00000647941.2:c.1172+51C= MANE Select	ENSP00000497326.1:n.1172+51C=
ENST00000264193.2:c.1172+51C=	ENSP00000264193.2:n.1172+51C=
ENST00000510489.1:n.422+51C=
ENST00000512905.5:c.58+51C=
NM_000097.5:c.1172+51C=	NP_000088.3:n.1172+51C=
XM_005247125.3:c.1172+51C=	XP_005247182.1:n.1172+51C=
NM_000097.7:c.1172+51C= MANE Select	NP_000088.3:n.1172+51C=
XM_005247125.4:c.1172+51C=	XP_005247182.1:n.1172+51C=
XR_001740025.2:n.1343+51C=
XR_001740026.1:n.1907+51C=
XR_001740027.1:n.1447+51C=
XR_001740028.1:n.1413+51C=