Canonical Allele Identifier: CA353644551

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98581406C>T , CM000665.2:g.98581406C>T	GRCh38
NC_000003.11:g.98300250C>T , CM000665.1:g.98300250C>T	GRCh37
NC_000003.10:g.99782940C>T	NCBI36
NG_015994.1:g.17206G>A
NG_015994.2:g.17206G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.163+1G>A
ENST00000647941.2:c.1277+1G>A MANE Select	ENSP00000497326.1:n.1277+1G>A
ENST00000264193.2:c.1277+1G>A	ENSP00000264193.2:n.1277+1G>A
ENST00000512905.5:c.163+1G>A
NM_000097.5:c.1277+1G>A	NP_000088.3:n.1277+1G>A
XM_005247125.3:c.1173-3136G>A	XP_005247182.1:n.1173-3136G>A
NM_000097.7:c.1277+1G>A MANE Select	NP_000088.3:n.1277+1G>A
XM_005247125.4:c.1173-3136G>A	XP_005247182.1:n.1173-3136G>A
XR_001740025.2:n.1344-3136G>A
XR_001740026.1:n.2012+1G>A
XR_001740027.1:n.1552+1G>A
XR_001740028.1:n.1518+1G>A