Canonical Allele Identifier: CA1805116386
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158057G= , CM000670.2:g.98158057G= GRCh38
NC_000008.10:g.99170285G= , CM000670.1:g.99170285G= GRCh37
NC_000008.9:g.99239461G= NCBI36
NG_052869.1:g.45765G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2861G= MANE Select ENSP00000385787.2:p.Arg954=
ENST00000349693.3:c.2861G= ENSP00000339529.3:p.Arg954=
ENST00000401707.6:c.2861G= ENSP00000385787.2:p.Arg954=
NM_001145860.1:c.2861G= NP_001139332.1:p.Arg954=
NM_001145861.1:c.2861G= NP_001139333.1:p.Arg954=
NM_015029.2:c.2861G= NP_055844.2:p.Arg954=
NM_001145860.2:c.2861G= MANE Select NP_001139332.1:p.Arg954=
NM_001145861.2:c.2861G= NP_001139333.1:p.Arg954=
NM_015029.3:c.2861G= NP_055844.2:p.Arg954=