Canonical Allele Identifier: CA371777696

Gene: POP1

Linked Data

• gnomAD v4: 8-98158101-C-T
• MyVariant Identifiers: chr8:g.99170329C>T (hg19) ; chr8:g.98158101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.98158101C>T , CM000670.2:g.98158101C>T	GRCh38
NC_000008.10:g.99170329C>T , CM000670.1:g.99170329C>T	GRCh37
NC_000008.9:g.99239505C>T	NCBI36
NG_052869.1:g.45809C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401707.7:c.2905C>T MANE Select	ENSP00000385787.2:p.Gln969Ter
ENST00000349693.3:c.2905C>T	ENSP00000339529.3:p.Gln969Ter
ENST00000401707.6:c.2905C>T	ENSP00000385787.2:p.Gln969Ter
NM_001145860.1:c.2905C>T	NP_001139332.1:p.Gln969Ter
NM_001145861.1:c.2905C>T	NP_001139333.1:p.Gln969Ter
NM_015029.2:c.2905C>T	NP_055844.2:p.Gln969Ter
NM_001145860.2:c.2905C>T MANE Select	NP_001139332.1:p.Gln969Ter
NM_001145861.2:c.2905C>T	NP_001139333.1:p.Gln969Ter
NM_015029.3:c.2905C>T	NP_055844.2:p.Gln969Ter