Canonical Allele Identifier: CA2053548594
Gene: POC1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89503544_89503584delinsGGGAAGTGAGGAGCGTCTCTGCCCGGCCACCATCCCGTCTA , CM000674.2:g.89503544_89503584delinsGGGAAGTGAGGAGCGTCTCTGCCCGGCCACCATCCCGTCTA GRCh38
NC_000012.11:g.89897321_89897361delinsGGGAAGTGAGGAGCGTCTCTGCCCGGCCACCATCCCGTCTA , CM000674.1:g.89897321_89897361delinsGGGAAGTGAGGAGCGTCTCTGCCCGGCCACCATCCCGTCTA GRCh37
NC_000012.10:g.88421452_88421492delinsGGGAAGTGAGGAGCGTCTCTGCCCGGCCACCATCCCGTCTA NCBI36
NG_041783.1:g.27679_27719delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000313546.8:c.101-6242_101-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC MANE Select ENSP00000323302.3:n.101-6242_101-6202delinsTAGACGGGATGGTGGCCG...
ENST00000313546.7:c.101-6242_101-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC ENSP00000323302.3:n.101-6242_101-6202delinsTAGACGGGATGGTGGCCG...
ENST00000393179.8:c.-118-11469_-118-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC ENSP00000376877.4:n.-118-11469_-118-11429delinsTAGACGGGATGGTG...
ENST00000539190.6:n.199-6242_199-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC
ENST00000546830.1:c.101-6242_101-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC ENSP00000449256.1:n.101-6242_101-6202delinsTAGACGGGATGGTGGCCG...
ENST00000547274.5:c.101-11469_101-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC ENSP00000449648.1:n.101-11469_101-11429delinsTAGACGGGATGGTGGC...
ENST00000547496.5:c.101-11469_101-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC ENSP00000447437.1:n.101-11469_101-11429delinsTAGACGGGATGGTGGC...
ENST00000548715.5:c.101-11469_101-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC ENSP00000449945.1:n.101-11469_101-11429delinsTAGACGGGATGGTGGC...
ENST00000549035.1:c.-26-6242_-26-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC ENSP00000447916.1:n.-26-6242_-26-6202delinsTAGACGGGATGGTGGCCG...
ENST00000549504.1:c.-118-11469_-118-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC ENSP00000450118.1:n.-118-11469_-118-11429delinsTAGACGGGATGGTG...
ENST00000552563.1:n.297-11469_297-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC
NM_001199777.1:c.-26-6242_-26-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC NP_001186706.1:n.-26-6242_-26-6202delinsTAGACGGGATGGTGGCCGGGC...
NM_172240.2:c.101-6242_101-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC NP_758440.1:n.101-6242_101-6202delinsTAGACGGGATGGTGGCCGGGCAGA...
NR_037659.1:n.468-11469_468-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC
NR_037660.1:n.449-11469_449-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC
NM_172240.3:c.101-6242_101-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC MANE Select NP_758440.1:n.101-6242_101-6202delinsTAGACGGGATGGTGGCCGGGCAGA...
NM_001199777.2:c.-26-6242_-26-6202delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC NP_001186706.1:n.-26-6242_-26-6202delinsTAGACGGGATGGTGGCCGGGC...
NR_037659.2:n.253-11469_253-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC
NR_037660.2:n.312-11469_312-11429delinsTAGACGGGATGGTGGCCGGGCAGAGACGCTCCTCACTTCCC