Canonical Allele Identifier: CA1805116620
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158159C= , CM000670.2:g.98158159C= GRCh38
NC_000008.10:g.99170387C= , CM000670.1:g.99170387C= GRCh37
NC_000008.9:g.99239563C= NCBI36
NG_052869.1:g.45867C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2963C= MANE Select ENSP00000385787.2:p.Thr988=
ENST00000349693.3:c.2963C= ENSP00000339529.3:p.Thr988=
ENST00000401707.6:c.2963C= ENSP00000385787.2:p.Thr988=
NM_001145860.1:c.2963C= NP_001139332.1:p.Thr988=
NM_001145861.1:c.2963C= NP_001139333.1:p.Thr988=
NM_015029.2:c.2963C= NP_055844.2:p.Thr988=
NM_001145860.2:c.2963C= MANE Select NP_001139332.1:p.Thr988=
NM_001145861.2:c.2963C= NP_001139333.1:p.Thr988=
NM_015029.3:c.2963C= NP_055844.2:p.Thr988=