Canonical Allele Identifier: CA2688039212
Gene: POP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158023_98158024dup , CM000670.2:g.98158023_98158024dup GRCh38
NC_000008.10:g.99170251_99170252dup , CM000670.1:g.99170251_99170252dup GRCh37
NC_000008.9:g.99239427_99239428dup NCBI36
NG_052869.1:g.45731_45732dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2827_2828dup MANE Select ENSP00000385787.2:p.Thr944Ter
ENST00000349693.3:c.2827_2828dup ENSP00000339529.3:p.Thr944Ter
ENST00000401707.6:c.2827_2828dup ENSP00000385787.2:p.Thr944Ter
NM_001145860.1:c.2827_2828dup NP_001139332.1:p.Thr944Ter
NM_001145861.1:c.2827_2828dup NP_001139333.1:p.Thr944Ter
NM_015029.2:c.2827_2828dup NP_055844.2:p.Thr944Ter
NM_001145860.2:c.2827_2828dup MANE Select NP_001139332.1:p.Thr944Ter
NM_001145861.2:c.2827_2828dup NP_001139333.1:p.Thr944Ter
NM_015029.3:c.2827_2828dup NP_055844.2:p.Thr944Ter