Canonical Allele Identifier: CA1805111157
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs1809419576

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148500del , CM000670.2:g.98148500del GRCh38
NC_000008.10:g.99160728del , CM000670.1:g.99160728del GRCh37
NC_000008.9:g.99229904del NCBI36
NG_052869.1:g.36208del

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-315del MANE Select ENSP00000385787.2:n.1711-315del
ENST00000349693.3:c.1711-315del ENSP00000339529.3:n.1711-315del
ENST00000401707.6:c.1711-315del ENSP00000385787.2:n.1711-315del
NM_001145860.1:c.1711-315del NP_001139332.1:n.1711-315del
NM_001145861.1:c.1711-315del NP_001139333.1:n.1711-315del
NM_015029.2:c.1711-315del NP_055844.2:n.1711-315del
XM_011516800.1:c.1711-315del XP_011515102.1:n.1711-315del
NM_001145860.2:c.1711-315del MANE Select NP_001139332.1:n.1711-315del
NM_001145861.2:c.1711-315del NP_001139333.1:n.1711-315del
NM_015029.3:c.1711-315del NP_055844.2:n.1711-315del