Canonical Allele Identifier: CA1116992002

Gene: POP1

Linked Data

• dbSNP Id: rs1809427921
• gnomAD v3: 8-98148658-C-A
• gnomAD v4: 8-98148658-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.98148658C>A , CM000670.2:g.98148658C>A	GRCh38
NC_000008.10:g.99160886C>A , CM000670.1:g.99160886C>A	GRCh37
NC_000008.9:g.99230062C>A	NCBI36
NG_052869.1:g.36366C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401707.7:c.1711-157C>A MANE Select	ENSP00000385787.2:n.1711-157C>A
ENST00000349693.3:c.1711-157C>A	ENSP00000339529.3:n.1711-157C>A
ENST00000401707.6:c.1711-157C>A	ENSP00000385787.2:n.1711-157C>A
NM_001145860.1:c.1711-157C>A	NP_001139332.1:n.1711-157C>A
NM_001145861.1:c.1711-157C>A	NP_001139333.1:n.1711-157C>A
NM_015029.2:c.1711-157C>A	NP_055844.2:n.1711-157C>A
XM_011516800.1:c.1711-157C>A	XP_011515102.1:n.1711-157C>A
NM_001145860.2:c.1711-157C>A MANE Select	NP_001139332.1:n.1711-157C>A
NM_001145861.2:c.1711-157C>A	NP_001139333.1:n.1711-157C>A
NM_015029.3:c.1711-157C>A	NP_055844.2:n.1711-157C>A