Canonical Allele Identifier: CA2688038526
Gene: POP1 HGNC NCBI

Linked Data

gnomAD v4: 8-98148674-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148674C>A , CM000670.2:g.98148674C>A GRCh38
NC_000008.10:g.99160902C>A , CM000670.1:g.99160902C>A GRCh37
NC_000008.9:g.99230078C>A NCBI36
NG_052869.1:g.36382C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.1711-141C>A MANE Select ENSP00000385787.2:n.1711-141C>A
ENST00000349693.3:c.1711-141C>A ENSP00000339529.3:n.1711-141C>A
ENST00000401707.6:c.1711-141C>A ENSP00000385787.2:n.1711-141C>A
NM_001145860.1:c.1711-141C>A NP_001139332.1:n.1711-141C>A
NM_001145861.1:c.1711-141C>A NP_001139333.1:n.1711-141C>A
NM_015029.2:c.1711-141C>A NP_055844.2:n.1711-141C>A
XM_011516800.1:c.1711-141C>A XP_011515102.1:n.1711-141C>A
NM_001145860.2:c.1711-141C>A MANE Select NP_001139332.1:n.1711-141C>A
NM_001145861.2:c.1711-141C>A NP_001139333.1:n.1711-141C>A
NM_015029.3:c.1711-141C>A NP_055844.2:n.1711-141C>A
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