Canonical Allele Identifier: CA1805111222
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148588_98148593delinsAATGAT , CM000670.2:g.98148588_98148593delinsAATGAT GRCh38
NC_000008.10:g.99160816_99160821delinsAATGAT , CM000670.1:g.99160816_99160821delinsAATGAT GRCh37
NC_000008.9:g.99229992_99229997delinsAATGAT NCBI36
NG_052869.1:g.36296_36301delinsAATGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-227_1711-222delinsAATGAT MANE Select ENSP00000385787.2:n.1711-227_1711-222delinsAATGAT
ENST00000349693.3:c.1711-227_1711-222delinsAATGAT ENSP00000339529.3:n.1711-227_1711-222delinsAATGAT
ENST00000401707.6:c.1711-227_1711-222delinsAATGAT ENSP00000385787.2:n.1711-227_1711-222delinsAATGAT
NM_001145860.1:c.1711-227_1711-222delinsAATGAT NP_001139332.1:n.1711-227_1711-222delinsAATGAT
NM_001145861.1:c.1711-227_1711-222delinsAATGAT NP_001139333.1:n.1711-227_1711-222delinsAATGAT
NM_015029.2:c.1711-227_1711-222delinsAATGAT NP_055844.2:n.1711-227_1711-222delinsAATGAT
XM_011516800.1:c.1711-227_1711-222delinsAATGAT XP_011515102.1:n.1711-227_1711-222delinsAATGAT
NM_001145860.2:c.1711-227_1711-222delinsAATGAT MANE Select NP_001139332.1:n.1711-227_1711-222delinsAATGAT
NM_001145861.2:c.1711-227_1711-222delinsAATGAT NP_001139333.1:n.1711-227_1711-222delinsAATGAT
NM_015029.3:c.1711-227_1711-222delinsAATGAT NP_055844.2:n.1711-227_1711-222delinsAATGAT