Canonical Allele Identifier: CA2053548570
Gene: POC1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89503532_89503572delinsGCCACCCCGTCTGGGAAGTGAGGAGCGTCTCTGCCCGGCCA , CM000674.2:g.89503532_89503572delinsGCCACCCCGTCTGGGAAGTGAGGAGCGTCTCTGCCCGGCCA GRCh38
NC_000012.11:g.89897309_89897349delinsGCCACCCCGTCTGGGAAGTGAGGAGCGTCTCTGCCCGGCCA , CM000674.1:g.89897309_89897349delinsGCCACCCCGTCTGGGAAGTGAGGAGCGTCTCTGCCCGGCCA GRCh37
NC_000012.10:g.88421440_88421480delinsGCCACCCCGTCTGGGAAGTGAGGAGCGTCTCTGCCCGGCCA NCBI36
NG_041783.1:g.27691_27731delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000313546.8:c.101-6230_101-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC MANE Select ENSP00000323302.3:n.101-6230_101-6190delinsTGGCCGGGCAGAGACGCT...
ENST00000313546.7:c.101-6230_101-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC ENSP00000323302.3:n.101-6230_101-6190delinsTGGCCGGGCAGAGACGCT...
ENST00000393179.8:c.-118-11457_-118-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC ENSP00000376877.4:n.-118-11457_-118-11417delinsTGGCCGGGCAGAGA...
ENST00000539190.6:n.199-6230_199-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC
ENST00000546830.1:c.101-6230_101-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC ENSP00000449256.1:n.101-6230_101-6190delinsTGGCCGGGCAGAGACGCT...
ENST00000547274.5:c.101-11457_101-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC ENSP00000449648.1:n.101-11457_101-11417delinsTGGCCGGGCAGAGACG...
ENST00000547496.5:c.101-11457_101-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC ENSP00000447437.1:n.101-11457_101-11417delinsTGGCCGGGCAGAGACG...
ENST00000548715.5:c.101-11457_101-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC ENSP00000449945.1:n.101-11457_101-11417delinsTGGCCGGGCAGAGACG...
ENST00000549035.1:c.-26-6230_-26-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC ENSP00000447916.1:n.-26-6230_-26-6190delinsTGGCCGGGCAGAGACGCT...
ENST00000549504.1:c.-118-11457_-118-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC ENSP00000450118.1:n.-118-11457_-118-11417delinsTGGCCGGGCAGAGA...
ENST00000552563.1:n.297-11457_297-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC
NM_001199777.1:c.-26-6230_-26-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC NP_001186706.1:n.-26-6230_-26-6190delinsTGGCCGGGCAGAGACGCTCCT...
NM_172240.2:c.101-6230_101-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC NP_758440.1:n.101-6230_101-6190delinsTGGCCGGGCAGAGACGCTCCTCAC...
NR_037659.1:n.468-11457_468-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC
NR_037660.1:n.449-11457_449-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC
NM_172240.3:c.101-6230_101-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC MANE Select NP_758440.1:n.101-6230_101-6190delinsTGGCCGGGCAGAGACGCTCCTCAC...
NM_001199777.2:c.-26-6230_-26-6190delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC NP_001186706.1:n.-26-6230_-26-6190delinsTGGCCGGGCAGAGACGCTCCT...
NR_037659.2:n.253-11457_253-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC
NR_037660.2:n.312-11457_312-11417delinsTGGCCGGGCAGAGACGCTCCTCACTTCCCAGACGGGGTGGC