Canonical Allele Identifier: CA2757611550
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585706_98585707insAACCAAACACACCCAA , CM000665.2:g.98585706_98585707insAACCAAACACACCCAA GRCh38
NC_000003.11:g.98304550_98304551insAACCAAACACACCCAA , CM000665.1:g.98304550_98304551insAACCAAACACACCCAA GRCh37
NC_000003.10:g.99787240_99787241insAACCAAACACACCCAA NCBI36
NG_015994.1:g.12906_12907insTGGGTGTGTTTGGTTT
NG_015994.2:g.12906_12907insTGGGTGTGTTTGGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-47_954-46insTGGGTGTGTTTGGTTT MANE Select ENSP00000497326.1:n.954-47_954-46insTGGGTGTGTTTGGTTT
ENST00000264193.2:c.954-47_954-46insTGGGTGTGTTTGGTTT ENSP00000264193.2:n.954-47_954-46insTGGGTGTGTTTGGTTT
ENST00000510489.1:n.157_158insTGGGTGTGTTTGGTTT
NM_000097.5:c.954-47_954-46insTGGGTGTGTTTGGTTT NP_000088.3:n.954-47_954-46insTGGGTGTGTTTGGTTT
XM_005247125.3:c.954-47_954-46insTGGGTGTGTTTGGTTT XP_005247182.1:n.954-47_954-46insTGGGTGTGTTTGGTTT
NM_000097.7:c.954-47_954-46insTGGGTGTGTTTGGTTT MANE Select NP_000088.3:n.954-47_954-46insTGGGTGTGTTTGGTTT
XM_005247125.4:c.954-47_954-46insTGGGTGTGTTTGGTTT XP_005247182.1:n.954-47_954-46insTGGGTGTGTTTGGTTT
XR_001740025.2:n.1125-47_1125-46insTGGGTGTGTTTGGTTT
XR_001740026.1:n.1642_1643insTGGGTGTGTTTGGTTT
XR_001740027.1:n.1229-47_1229-46insTGGGTGTGTTTGGTTT
XR_001740028.1:n.1195-47_1195-46insTGGGTGTGTTTGGTTT