Canonical Allele Identifier: CA1805116104
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157844_98157845delinsTC , CM000670.2:g.98157844_98157845delinsTC GRCh38
NC_000008.10:g.99170072_99170073delinsTC , CM000670.1:g.99170072_99170073delinsTC GRCh37
NC_000008.9:g.99239248_99239249delinsTC NCBI36
NG_052869.1:g.45552_45553delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2648_2649delinsTC MANE Select ENSP00000385787.2:p.Phe883=
ENST00000349693.3:c.2648_2649delinsTC ENSP00000339529.3:p.Phe883=
ENST00000401707.6:c.2648_2649delinsTC ENSP00000385787.2:p.Phe883=
NM_001145860.1:c.2648_2649delinsTC NP_001139332.1:p.Phe883=
NM_001145861.1:c.2648_2649delinsTC NP_001139333.1:p.Phe883=
NM_015029.2:c.2648_2649delinsTC NP_055844.2:p.Phe883=
NM_001145860.2:c.2648_2649delinsTC MANE Select NP_001139332.1:p.Phe883=
NM_001145861.2:c.2648_2649delinsTC NP_001139333.1:p.Phe883=
NM_015029.3:c.2648_2649delinsTC NP_055844.2:p.Phe883=