Canonical Allele Identifier: CA1805111456
Community Standard Title: NM_001145860.2(POP1):c.1748G= (p.Gly583=)
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148852G= , CM000670.2:g.98148852G= GRCh38
NC_000008.10:g.99161080G= , CM000670.1:g.99161080G= GRCh37
NC_000008.9:g.99230256G= NCBI36
NG_052869.1:g.36560G=

Transcript Alleles

HGVS Amino-acid Change
NM_001145860.2:c.1748G= MANE Select NP_001139332.1:p.Gly583=
ENST00000401707.7:c.1748G= MANE Select ENSP00000385787.2:p.Gly583=
NM_001145860.1:c.1748G= NP_001139332.1:p.Gly583=
NM_001145861.1:c.1748G= NP_001139333.1:p.Gly583=
NM_001145861.2:c.1748G= NP_001139333.1:p.Gly583=
NM_015029.2:c.1748G= NP_055844.2:p.Gly583=
NM_015029.3:c.1748G= NP_055844.2:p.Gly583=
ENST00000349693.3:c.1748G= ENSP00000339529.3:p.Gly583=
ENST00000401707.6:c.1748G= ENSP00000385787.2:p.Gly583=
XM_011516800.1:c.1748G= XP_011515102.1:p.Gly583=