Canonical Allele Identifier: CA2688038585
Gene: POP1 HGNC NCBI

Linked Data

gnomAD v4: 8-98148760-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98148760A>G , CM000670.2:g.98148760A>G GRCh38
NC_000008.10:g.99160988A>G , CM000670.1:g.99160988A>G GRCh37
NC_000008.9:g.99230164A>G NCBI36
NG_052869.1:g.36468A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000401707.7:c.1711-55A>G MANE Select ENSP00000385787.2:n.1711-55A>G
ENST00000349693.3:c.1711-55A>G ENSP00000339529.3:n.1711-55A>G
ENST00000401707.6:c.1711-55A>G ENSP00000385787.2:n.1711-55A>G
NM_001145860.1:c.1711-55A>G NP_001139332.1:n.1711-55A>G
NM_001145861.1:c.1711-55A>G NP_001139333.1:n.1711-55A>G
NM_015029.2:c.1711-55A>G NP_055844.2:n.1711-55A>G
XM_011516800.1:c.1711-55A>G XP_011515102.1:n.1711-55A>G
NM_001145860.2:c.1711-55A>G MANE Select NP_001139332.1:n.1711-55A>G
NM_001145861.2:c.1711-55A>G NP_001139333.1:n.1711-55A>G
NM_015029.3:c.1711-55A>G NP_055844.2:n.1711-55A>G