Canonical Allele Identifier: CA1805115776
Gene: POP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157613G= , CM000670.2:g.98157613G= GRCh38
NC_000008.10:g.99169841G= , CM000670.1:g.99169841G= GRCh37
NC_000008.9:g.99239017G= NCBI36
NG_052869.1:g.45321G=

Transcript Alleles

HGVS Amino-acid change
ENST00000401707.7:c.2421-4G= MANE Select ENSP00000385787.2:n.2421-4G=
ENST00000349693.3:c.2421-4G= ENSP00000339529.3:n.2421-4G=
ENST00000401707.6:c.2421-4G= ENSP00000385787.2:n.2421-4G=
ENST00000517435.1:n.456-4G=
NM_001145860.1:c.2421-4G= NP_001139332.1:n.2421-4G=
NM_001145861.1:c.2421-4G= NP_001139333.1:n.2421-4G=
NM_015029.2:c.2421-4G= NP_055844.2:n.2421-4G=
NM_001145860.2:c.2421-4G= MANE Select NP_001139332.1:n.2421-4G=
NM_001145861.2:c.2421-4G= NP_001139333.1:n.2421-4G=
NM_015029.3:c.2421-4G= NP_055844.2:n.2421-4G=
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