Canonical Allele Identifier: CA1805116681
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158181C= , CM000670.2:g.98158181C= GRCh38
NC_000008.10:g.99170409C= , CM000670.1:g.99170409C= GRCh37
NC_000008.9:g.99239585C= NCBI36
NG_052869.1:g.45889C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2985C= MANE Select ENSP00000385787.2:p.Ser995=
ENST00000349693.3:c.2985C= ENSP00000339529.3:p.Ser995=
ENST00000401707.6:c.2985C= ENSP00000385787.2:p.Ser995=
NM_001145860.1:c.2985C= NP_001139332.1:p.Ser995=
NM_001145861.1:c.2985C= NP_001139333.1:p.Ser995=
NM_015029.2:c.2985C= NP_055844.2:p.Ser995=
NM_001145860.2:c.2985C= MANE Select NP_001139332.1:p.Ser995=
NM_001145861.2:c.2985C= NP_001139333.1:p.Ser995=
NM_015029.3:c.2985C= NP_055844.2:p.Ser995=