Canonical Allele Identifier: CA2839258690
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157982_98157984del , CM000670.2:g.98157982_98157984del GRCh38
NC_000008.10:g.99170210_99170212del , CM000670.1:g.99170210_99170212del GRCh37
NC_000008.9:g.99239386_99239388del NCBI36
NG_052869.1:g.45690_45692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2786_2788del MANE Select ENSP00000385787.2:p.Asp929del
ENST00000349693.3:c.2786_2788del ENSP00000339529.3:p.Asp929del
ENST00000401707.6:c.2786_2788del ENSP00000385787.2:p.Asp929del
NM_001145860.1:c.2786_2788del NP_001139332.1:p.Asp929del
NM_001145861.1:c.2786_2788del NP_001139333.1:p.Asp929del
NM_015029.2:c.2786_2788del NP_055844.2:p.Asp929del
NM_001145860.2:c.2786_2788del MANE Select NP_001139332.1:p.Asp929del
NM_001145861.2:c.2786_2788del NP_001139333.1:p.Asp929del
NM_015029.3:c.2786_2788del NP_055844.2:p.Asp929del