Canonical Allele Identifier: CA1387393813

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585688G= , CM000665.2:g.98585688G=	GRCh38
NC_000003.11:g.98304532G= , CM000665.1:g.98304532G=	GRCh37
NC_000003.10:g.99787222G=	NCBI36
NG_015994.1:g.12924C=
NG_015994.2:g.12924C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.954-29C= MANE Select	ENSP00000497326.1:n.954-29C=
ENST00000264193.2:c.954-29C=	ENSP00000264193.2:n.954-29C=
ENST00000510489.1:n.175C=
NM_000097.5:c.954-29C=	NP_000088.3:n.954-29C=
XM_005247125.3:c.954-29C=	XP_005247182.1:n.954-29C=
NM_000097.7:c.954-29C= MANE Select	NP_000088.3:n.954-29C=
XM_005247125.4:c.954-29C=	XP_005247182.1:n.954-29C=
XR_001740025.2:n.1125-29C=
XR_001740026.1:n.1660C=
XR_001740027.1:n.1229-29C=
XR_001740028.1:n.1195-29C=