Canonical Allele Identifier: CA2688038541
Gene: POP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148701del , CM000670.2:g.98148701del GRCh38
NC_000008.10:g.99160929del , CM000670.1:g.99160929del GRCh37
NC_000008.9:g.99230105del NCBI36
NG_052869.1:g.36409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-114del MANE Select ENSP00000385787.2:n.1711-114del
ENST00000349693.3:c.1711-114del ENSP00000339529.3:n.1711-114del
ENST00000401707.6:c.1711-114del ENSP00000385787.2:n.1711-114del
NM_001145860.1:c.1711-114del NP_001139332.1:n.1711-114del
NM_001145861.1:c.1711-114del NP_001139333.1:n.1711-114del
NM_015029.2:c.1711-114del NP_055844.2:n.1711-114del
XM_011516800.1:c.1711-114del XP_011515102.1:n.1711-114del
NM_001145860.2:c.1711-114del MANE Select NP_001139332.1:n.1711-114del
NM_001145861.2:c.1711-114del NP_001139333.1:n.1711-114del
NM_015029.3:c.1711-114del NP_055844.2:n.1711-114del