Canonical Allele Identifier: CA1805116148
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157889C= , CM000670.2:g.98157889C= GRCh38
NC_000008.10:g.99170117C= , CM000670.1:g.99170117C= GRCh37
NC_000008.9:g.99239293C= NCBI36
NG_052869.1:g.45597C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2693C= MANE Select ENSP00000385787.2:p.Ser898=
ENST00000349693.3:c.2693C= ENSP00000339529.3:p.Ser898=
ENST00000401707.6:c.2693C= ENSP00000385787.2:p.Ser898=
NM_001145860.1:c.2693C= NP_001139332.1:p.Ser898=
NM_001145861.1:c.2693C= NP_001139333.1:p.Ser898=
NM_015029.2:c.2693C= NP_055844.2:p.Ser898=
NM_001145860.2:c.2693C= MANE Select NP_001139332.1:p.Ser898=
NM_001145861.2:c.2693C= NP_001139333.1:p.Ser898=
NM_015029.3:c.2693C= NP_055844.2:p.Ser898=