Canonical Allele Identifier: CA1805115716
Gene: POP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157555C= , CM000670.2:g.98157555C= GRCh38
NC_000008.10:g.99169783C= , CM000670.1:g.99169783C= GRCh37
NC_000008.9:g.99238959C= NCBI36
NG_052869.1:g.45263C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2421-62C= MANE Select ENSP00000385787.2:n.2421-62C=
ENST00000349693.3:c.2421-62C= ENSP00000339529.3:n.2421-62C=
ENST00000401707.6:c.2421-62C= ENSP00000385787.2:n.2421-62C=
ENST00000517435.1:n.456-62C=
NM_001145860.1:c.2421-62C= NP_001139332.1:n.2421-62C=
NM_001145861.1:c.2421-62C= NP_001139333.1:n.2421-62C=
NM_015029.2:c.2421-62C= NP_055844.2:n.2421-62C=
NM_001145860.2:c.2421-62C= MANE Select NP_001139332.1:n.2421-62C=
NM_001145861.2:c.2421-62C= NP_001139333.1:n.2421-62C=
NM_015029.3:c.2421-62C= NP_055844.2:n.2421-62C=
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