Canonical Allele Identifier: CA353645216

Gene: CPOX

Linked Data

• MyVariant Identifiers: chr3:g.98304483A>G (hg19) ; chr3:g.98585639A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585639A>G , CM000665.2:g.98585639A>G	GRCh38
NC_000003.11:g.98304483A>G , CM000665.1:g.98304483A>G	GRCh37
NC_000003.10:g.99787173A>G	NCBI36
NG_015994.1:g.12973T>C
NG_015994.2:g.12973T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.974T>C MANE Select	ENSP00000497326.1:p.Ile325Thr
ENST00000264193.2:c.974T>C	ENSP00000264193.2:p.Ile325Thr
ENST00000510489.1:n.224T>C
NM_000097.5:c.974T>C	NP_000088.3:p.Ile325Thr
XM_005247125.3:c.974T>C	XP_005247182.1:p.Ile325Thr
NM_000097.7:c.974T>C MANE Select	NP_000088.3:p.Ile325Thr
XM_005247125.4:c.974T>C	XP_005247182.1:p.Ile325Thr
XR_001740025.2:n.1145T>C
XR_001740026.1:n.1709T>C
XR_001740027.1:n.1249T>C
XR_001740028.1:n.1215T>C