Canonical Allele Identifier: CA1805116539
Gene: POP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158108A= , CM000670.2:g.98158108A= GRCh38
NC_000008.10:g.99170336A= , CM000670.1:g.99170336A= GRCh37
NC_000008.9:g.99239512A= NCBI36
NG_052869.1:g.45816A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2912A= MANE Select ENSP00000385787.2:p.Asp971=
ENST00000349693.3:c.2912A= ENSP00000339529.3:p.Asp971=
ENST00000401707.6:c.2912A= ENSP00000385787.2:p.Asp971=
NM_001145860.1:c.2912A= NP_001139332.1:p.Asp971=
NM_001145861.1:c.2912A= NP_001139333.1:p.Asp971=
NM_015029.2:c.2912A= NP_055844.2:p.Asp971=
NM_001145860.2:c.2912A= MANE Select NP_001139332.1:p.Asp971=
NM_001145861.2:c.2912A= NP_001139333.1:p.Asp971=
NM_015029.3:c.2912A= NP_055844.2:p.Asp971=