Canonical Allele Identifier: CA462457491

Gene: POP1

Linked Data

• MyVariant Identifiers: chr8:g.99170355C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.98158127C>G , CM000670.2:g.98158127C>G	GRCh38
NC_000008.10:g.99170355C>G , CM000670.1:g.99170355C>G	GRCh37
NC_000008.9:g.99239531C>G	NCBI36
NG_052869.1:g.45835C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401707.7:c.2931C>G MANE Select	ENSP00000385787.2:p.Gly977=
ENST00000349693.3:c.2931C>G	ENSP00000339529.3:p.Gly977=
ENST00000401707.6:c.2931C>G	ENSP00000385787.2:p.Gly977=
NM_001145860.1:c.2931C>G	NP_001139332.1:p.Gly977=
NM_001145861.1:c.2931C>G	NP_001139333.1:p.Gly977=
NM_015029.2:c.2931C>G	NP_055844.2:p.Gly977=
NM_001145860.2:c.2931C>G MANE Select	NP_001139332.1:p.Gly977=
NM_001145861.2:c.2931C>G	NP_001139333.1:p.Gly977=
NM_015029.3:c.2931C>G	NP_055844.2:p.Gly977=