Canonical Allele Identifier: CA11370405
Community Standard Title: NM_000097.7(CPOX):c.812-246C>T
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98589100G>A , CM000665.2:g.98589100G>A GRCh38
NC_000003.11:g.98307944G>A , CM000665.1:g.98307944G>A GRCh37
NC_000003.10:g.99790634G>A NCBI36
NG_015994.1:g.9512C>T
NG_015994.2:g.9512C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000097.7:c.812-246C>T MANE Select NP_000088.3:n.812-246C>T
ENST00000647941.2:c.812-246C>T MANE Select ENSP00000497326.1:n.812-246C>T
NM_000097.5:c.812-246C>T NP_000088.3:n.812-246C>T
ENST00000264193.2:c.812-246C>T ENSP00000264193.2:n.812-246C>T
XM_005247125.3:c.812-246C>T XP_005247182.1:n.812-246C>T
XM_005247125.4:c.812-246C>T XP_005247182.1:n.812-246C>T
XM_011512437.1:c.812-246C>T XP_011510739.1:n.812-246C>T
XR_001740025.2:n.983-246C>T
XR_001740026.1:n.988-246C>T
XR_001740027.1:n.1087-246C>T
XR_001740028.1:n.1053-246C>T