Canonical Allele Identifier: CA1805111210
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148578A= , CM000670.2:g.98148578A= GRCh38
NC_000008.10:g.99160806A= , CM000670.1:g.99160806A= GRCh37
NC_000008.9:g.99229982A= NCBI36
NG_052869.1:g.36286A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-237A= MANE Select ENSP00000385787.2:n.1711-237A=
ENST00000349693.3:c.1711-237A= ENSP00000339529.3:n.1711-237A=
ENST00000401707.6:c.1711-237A= ENSP00000385787.2:n.1711-237A=
NM_001145860.1:c.1711-237A= NP_001139332.1:n.1711-237A=
NM_001145861.1:c.1711-237A= NP_001139333.1:n.1711-237A=
NM_015029.2:c.1711-237A= NP_055844.2:n.1711-237A=
XM_011516800.1:c.1711-237A= XP_011515102.1:n.1711-237A=
NM_001145860.2:c.1711-237A= MANE Select NP_001139332.1:n.1711-237A=
NM_001145861.2:c.1711-237A= NP_001139333.1:n.1711-237A=
NM_015029.3:c.1711-237A= NP_055844.2:n.1711-237A=