Canonical Allele Identifier: CA12733635
Community Standard Title: NM_001145860.2(POP1):c.824-95A>C
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98134377A>C , CM000670.2:g.98134377A>C GRCh38
NC_000008.10:g.99146605A>C , CM000670.1:g.99146605A>C GRCh37
NC_000008.9:g.99215781A>C NCBI36
NG_052869.1:g.22085A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001145860.2:c.824-95A>C MANE Select NP_001139332.1:n.824-95A>C
ENST00000401707.7:c.824-95A>C MANE Select ENSP00000385787.2:n.824-95A>C
NM_001145860.1:c.824-95A>C NP_001139332.1:n.824-95A>C
NM_001145861.1:c.824-95A>C NP_001139333.1:n.824-95A>C
NM_001145861.2:c.824-95A>C NP_001139333.1:n.824-95A>C
NM_015029.2:c.824-95A>C NP_055844.2:n.824-95A>C
NM_015029.3:c.824-95A>C NP_055844.2:n.824-95A>C
ENST00000349693.3:c.824-95A>C ENSP00000339529.3:n.824-95A>C
ENST00000401707.6:c.824-95A>C ENSP00000385787.2:n.824-95A>C
XM_011516800.1:c.824-95A>C XP_011515102.1:n.824-95A>C
XM_011516801.1:c.824-95A>C XP_011515103.1:n.824-95A>C
XM_011516801.2:c.824-95A>C XP_011515103.1:n.824-95A>C