Canonical Allele Identifier: CA353645149

Gene: CPOX

Linked Data

• MyVariant Identifiers: chr3:g.98304447A>G (hg19) ; chr3:g.98585603A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585603A>G , CM000665.2:g.98585603A>G	GRCh38
NC_000003.11:g.98304447A>G , CM000665.1:g.98304447A>G	GRCh37
NC_000003.10:g.99787137A>G	NCBI36
NG_015994.1:g.13009T>C
NG_015994.2:g.13009T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.1010T>C MANE Select	ENSP00000497326.1:p.Ile337Thr
ENST00000264193.2:c.1010T>C	ENSP00000264193.2:p.Ile337Thr
ENST00000510489.1:n.260T>C
NM_000097.5:c.1010T>C	NP_000088.3:p.Ile337Thr
XM_005247125.3:c.1010T>C	XP_005247182.1:p.Ile337Thr
NM_000097.7:c.1010T>C MANE Select	NP_000088.3:p.Ile337Thr
XM_005247125.4:c.1010T>C	XP_005247182.1:p.Ile337Thr
XR_001740025.2:n.1181T>C
XR_001740026.1:n.1745T>C
XR_001740027.1:n.1285T>C
XR_001740028.1:n.1251T>C