Canonical Allele Identifier: CA11370406

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98590310G>C , CM000665.2:g.98590310G>C	GRCh38
NC_000003.11:g.98309154G>C , CM000665.1:g.98309154G>C	GRCh37
NC_000003.10:g.99791844G>C	NCBI36
NG_015994.1:g.8302C>G
NG_015994.2:g.8302C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.811+322C>G MANE Select	ENSP00000497326.1:n.811+322C>G
ENST00000264193.2:c.811+322C>G	ENSP00000264193.2:n.811+322C>G
ENST00000513674.1:c.*59+322C>G	ENSP00000424924.1:n.*59+322C>G
NM_000097.5:c.811+322C>G	NP_000088.3:n.811+322C>G
XM_005247125.3:c.811+322C>G	XP_005247182.1:n.811+322C>G
XM_011512437.1:c.811+322C>G	XP_011510739.1:n.811+322C>G
NM_000097.7:c.811+322C>G MANE Select	NP_000088.3:n.811+322C>G
XM_005247125.4:c.811+322C>G	XP_005247182.1:n.811+322C>G
XR_001740025.2:n.982+322C>G
XR_001740026.1:n.987+322C>G
XR_001740027.1:n.991+322C>G
XR_001740028.1:n.991+322C>G