Canonical Allele Identifier: CA1805115955
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157726G= , CM000670.2:g.98157726G= GRCh38
NC_000008.10:g.99169954G= , CM000670.1:g.99169954G= GRCh37
NC_000008.9:g.99239130G= NCBI36
NG_052869.1:g.45434G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2530G= MANE Select ENSP00000385787.2:p.Ala844=
ENST00000349693.3:c.2530G= ENSP00000339529.3:p.Ala844=
ENST00000401707.6:c.2530G= ENSP00000385787.2:p.Ala844=
NM_001145860.1:c.2530G= NP_001139332.1:p.Ala844=
NM_001145861.1:c.2530G= NP_001139333.1:p.Ala844=
NM_015029.2:c.2530G= NP_055844.2:p.Ala844=
NM_001145860.2:c.2530G= MANE Select NP_001139332.1:p.Ala844=
NM_001145861.2:c.2530G= NP_001139333.1:p.Ala844=
NM_015029.3:c.2530G= NP_055844.2:p.Ala844=