Canonical Allele Identifier: CA1805116530
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158106A= , CM000670.2:g.98158106A= GRCh38
NC_000008.10:g.99170334A= , CM000670.1:g.99170334A= GRCh37
NC_000008.9:g.99239510A= NCBI36
NG_052869.1:g.45814A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2910A= MANE Select ENSP00000385787.2:p.Gly970=
ENST00000349693.3:c.2910A= ENSP00000339529.3:p.Gly970=
ENST00000401707.6:c.2910A= ENSP00000385787.2:p.Gly970=
NM_001145860.1:c.2910A= NP_001139332.1:p.Gly970=
NM_001145861.1:c.2910A= NP_001139333.1:p.Gly970=
NM_015029.2:c.2910A= NP_055844.2:p.Gly970=
NM_001145860.2:c.2910A= MANE Select NP_001139332.1:p.Gly970=
NM_001145861.2:c.2910A= NP_001139333.1:p.Gly970=
NM_015029.3:c.2910A= NP_055844.2:p.Gly970=