Canonical Allele Identifier: CA1387399114

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98591089G= , CM000665.2:g.98591089G=	GRCh38
NC_000003.11:g.98309933G= , CM000665.1:g.98309933G=	GRCh37
NC_000003.10:g.99792623G=	NCBI36
NG_015994.1:g.7523C=
NG_015994.2:g.7523C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.623C= MANE Select	ENSP00000497326.1:p.Ser208=
ENST00000264193.2:c.623C=	ENSP00000264193.2:p.Ser208=
ENST00000513674.1:c.508-24C=	ENSP00000424924.1:n.508-24C=
ENST00000515041.1:n.729C=
NM_000097.5:c.623C=	NP_000088.3:p.Ser208=
XM_005247125.3:c.623C=	XP_005247182.1:p.Ser208=
XM_011512437.1:c.623C=	XP_011510739.1:p.Ser208=
NM_000097.7:c.623C= MANE Select	NP_000088.3:p.Ser208=
XM_005247125.4:c.623C=	XP_005247182.1:p.Ser208=
XR_001740025.2:n.794C=
XR_001740026.1:n.799C=
XR_001740027.1:n.803C=
XR_001740028.1:n.803C=