Canonical Allele Identifier: CA1387406167

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98581474T= , CM000665.2:g.98581474T=	GRCh38
NC_000003.11:g.98300318T= , CM000665.1:g.98300318T=	GRCh37
NC_000003.10:g.99783008T=	NCBI36
NG_015994.1:g.17138A=
NG_015994.2:g.17138A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.96A=
ENST00000647941.2:c.1210A= MANE Select	ENSP00000497326.1:p.Lys404=
ENST00000264193.2:c.1210A=	ENSP00000264193.2:p.Lys404=
ENST00000510489.1:n.460A=
ENST00000512905.5:c.96A=
NM_000097.5:c.1210A=	NP_000088.3:p.Lys404=
XM_005247125.3:c.1173-3204A=	XP_005247182.1:n.1173-3204A=
NM_000097.7:c.1210A= MANE Select	NP_000088.3:p.Lys404=
XM_005247125.4:c.1173-3204A=	XP_005247182.1:n.1173-3204A=
XR_001740025.2:n.1344-3204A=
XR_001740026.1:n.1945A=
XR_001740027.1:n.1485A=
XR_001740028.1:n.1451A=