Canonical Allele Identifier: CA353644875

Gene: CPOX

Linked Data

• gnomAD v4: 3-98585481-T-C
• MyVariant Identifiers: chr3:g.98304325T>C (hg19) ; chr3:g.98585481T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585481T>C , CM000665.2:g.98585481T>C	GRCh38
NC_000003.11:g.98304325T>C , CM000665.1:g.98304325T>C	GRCh37
NC_000003.10:g.99787015T>C	NCBI36
NG_015994.1:g.13131A>G
NG_015994.2:g.13131A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.18A>G
ENST00000647941.2:c.1132A>G MANE Select	ENSP00000497326.1:p.Thr378Ala
ENST00000264193.2:c.1132A>G	ENSP00000264193.2:p.Thr378Ala
ENST00000510489.1:n.382A>G
ENST00000512905.5:c.18A>G
NM_000097.5:c.1132A>G	NP_000088.3:p.Thr378Ala
XM_005247125.3:c.1132A>G	XP_005247182.1:p.Thr378Ala
NM_000097.7:c.1132A>G MANE Select	NP_000088.3:p.Thr378Ala
XM_005247125.4:c.1132A>G	XP_005247182.1:p.Thr378Ala
XR_001740025.2:n.1303A>G
XR_001740026.1:n.1867A>G
XR_001740027.1:n.1407A>G
XR_001740028.1:n.1373A>G