Canonical Allele Identifier: CA1805111125
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148460_98148462delinsTCA , CM000670.2:g.98148460_98148462delinsTCA GRCh38
NC_000008.10:g.99160688_99160690delinsTCA , CM000670.1:g.99160688_99160690delinsTCA GRCh37
NC_000008.9:g.99229864_99229866delinsTCA NCBI36
NG_052869.1:g.36168_36170delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-355_1711-353delinsTCA MANE Select ENSP00000385787.2:n.1711-355_1711-353delinsTCA
ENST00000349693.3:c.1711-355_1711-353delinsTCA ENSP00000339529.3:n.1711-355_1711-353delinsTCA
ENST00000401707.6:c.1711-355_1711-353delinsTCA ENSP00000385787.2:n.1711-355_1711-353delinsTCA
NM_001145860.1:c.1711-355_1711-353delinsTCA NP_001139332.1:n.1711-355_1711-353delinsTCA
NM_001145861.1:c.1711-355_1711-353delinsTCA NP_001139333.1:n.1711-355_1711-353delinsTCA
NM_015029.2:c.1711-355_1711-353delinsTCA NP_055844.2:n.1711-355_1711-353delinsTCA
XM_011516800.1:c.1711-355_1711-353delinsTCA XP_011515102.1:n.1711-355_1711-353delinsTCA
NM_001145860.2:c.1711-355_1711-353delinsTCA MANE Select NP_001139332.1:n.1711-355_1711-353delinsTCA
NM_001145861.2:c.1711-355_1711-353delinsTCA NP_001139333.1:n.1711-355_1711-353delinsTCA
NM_015029.3:c.1711-355_1711-353delinsTCA NP_055844.2:n.1711-355_1711-353delinsTCA