Canonical Allele Identifier: CA1805115780
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157615A= , CM000670.2:g.98157615A= GRCh38
NC_000008.10:g.99169843A= , CM000670.1:g.99169843A= GRCh37
NC_000008.9:g.99239019A= NCBI36
NG_052869.1:g.45323A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2421-2A= MANE Select ENSP00000385787.2:n.2421-2A=
ENST00000349693.3:c.2421-2A= ENSP00000339529.3:n.2421-2A=
ENST00000401707.6:c.2421-2A= ENSP00000385787.2:n.2421-2A=
ENST00000517435.1:n.456-2A=
NM_001145860.1:c.2421-2A= NP_001139332.1:n.2421-2A=
NM_001145861.1:c.2421-2A= NP_001139333.1:n.2421-2A=
NM_015029.2:c.2421-2A= NP_055844.2:n.2421-2A=
NM_001145860.2:c.2421-2A= MANE Select NP_001139332.1:n.2421-2A=
NM_001145861.2:c.2421-2A= NP_001139333.1:n.2421-2A=
NM_015029.3:c.2421-2A= NP_055844.2:n.2421-2A=