Canonical Allele Identifier: CA353644885

Gene: CPOX

Linked Data

• MyVariant Identifiers: chr3:g.98304330G>T (hg19) ; chr3:g.98585486G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585486G>T , CM000665.2:g.98585486G>T	GRCh38
NC_000003.11:g.98304330G>T , CM000665.1:g.98304330G>T	GRCh37
NC_000003.10:g.99787020G>T	NCBI36
NG_015994.1:g.13126C>A
NG_015994.2:g.13126C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.13C>A
ENST00000647941.2:c.1127C>A MANE Select	ENSP00000497326.1:p.Ser376Ter
ENST00000264193.2:c.1127C>A	ENSP00000264193.2:p.Ser376Ter
ENST00000510489.1:n.377C>A
ENST00000512905.5:c.13C>A
NM_000097.5:c.1127C>A	NP_000088.3:p.Ser376Ter
XM_005247125.3:c.1127C>A	XP_005247182.1:p.Ser376Ter
NM_000097.7:c.1127C>A MANE Select	NP_000088.3:p.Ser376Ter
XM_005247125.4:c.1127C>A	XP_005247182.1:p.Ser376Ter
XR_001740025.2:n.1298C>A
XR_001740026.1:n.1862C>A
XR_001740027.1:n.1402C>A
XR_001740028.1:n.1368C>A