Canonical Allele Identifier: CA1116991970

Gene: POP1

Linked Data

• dbSNP Id: rs1809417902
• gnomAD v3: 8-98148460-TCA-T
• gnomAD v4: 8-98148460-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.98148462_98148463del , CM000670.2:g.98148462_98148463del	GRCh38
NC_000008.10:g.99160690_99160691del , CM000670.1:g.99160690_99160691del	GRCh37
NC_000008.9:g.99229866_99229867del	NCBI36
NG_052869.1:g.36170_36171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401707.7:c.1711-353_1711-352del MANE Select	ENSP00000385787.2:n.1711-353_1711-352del
ENST00000349693.3:c.1711-353_1711-352del	ENSP00000339529.3:n.1711-353_1711-352del
ENST00000401707.6:c.1711-353_1711-352del	ENSP00000385787.2:n.1711-353_1711-352del
NM_001145860.1:c.1711-353_1711-352del	NP_001139332.1:n.1711-353_1711-352del
NM_001145861.1:c.1711-353_1711-352del	NP_001139333.1:n.1711-353_1711-352del
NM_015029.2:c.1711-353_1711-352del	NP_055844.2:n.1711-353_1711-352del
XM_011516800.1:c.1711-353_1711-352del	XP_011515102.1:n.1711-353_1711-352del
NM_001145860.2:c.1711-353_1711-352del MANE Select	NP_001139332.1:n.1711-353_1711-352del
NM_001145861.2:c.1711-353_1711-352del	NP_001139333.1:n.1711-353_1711-352del
NM_015029.3:c.1711-353_1711-352del	NP_055844.2:n.1711-353_1711-352del