Canonical Allele Identifier: CA1387393833
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585705_98585706delinsCA , CM000665.2:g.98585705_98585706delinsCA GRCh38
NC_000003.11:g.98304549_98304550delinsCA , CM000665.1:g.98304549_98304550delinsCA GRCh37
NC_000003.10:g.99787239_99787240delinsCA NCBI36
NG_015994.1:g.12906_12907delinsTG
NG_015994.2:g.12906_12907delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-47_954-46delinsTG MANE Select ENSP00000497326.1:n.954-47_954-46delinsTG
ENST00000264193.2:c.954-47_954-46delinsTG ENSP00000264193.2:n.954-47_954-46delinsTG
ENST00000510489.1:n.157_158delinsTG
NM_000097.5:c.954-47_954-46delinsTG NP_000088.3:n.954-47_954-46delinsTG
XM_005247125.3:c.954-47_954-46delinsTG XP_005247182.1:n.954-47_954-46delinsTG
NM_000097.7:c.954-47_954-46delinsTG MANE Select NP_000088.3:n.954-47_954-46delinsTG
XM_005247125.4:c.954-47_954-46delinsTG XP_005247182.1:n.954-47_954-46delinsTG
XR_001740025.2:n.1125-47_1125-46delinsTG
XR_001740026.1:n.1642_1643delinsTG
XR_001740027.1:n.1229-47_1229-46delinsTG
XR_001740028.1:n.1195-47_1195-46delinsTG