Canonical Allele Identifier: CA541487628

Gene: PLCL2

Linked Data

• dbSNP Id: rs1372653821
• gnomAD v2: 3-16938658-C-CT
• gnomAD v3: 3-16897160-C-CT
• gnomAD v4: 3-16897160-C-CT
• MyVariant Identifiers: chr3:g.16938658_16938659insT (hg19) ; chr3:g.16897160_16897161insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16897166dup , CM000665.2:g.16897166dup	GRCh38
NC_000003.11:g.16938664dup , CM000665.1:g.16938664dup	GRCh37
NC_000003.10:g.16913668dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615277.5:c.327+11800dup MANE Select	ENSP00000478458.1:n.327+11800dup
ENST00000460467.1:n.438+94078dup
ENST00000615277.4:c.327+11800dup	ENSP00000478458.1:n.327+11800dup
NM_001144382.1:c.327+11800dup	NP_001137854.1:n.327+11800dup
XM_006713073.3:c.-2507dup	XP_006713136.1:n.-2507dup
XM_017006022.2:c.327+11800dup	XP_016861511.1:n.327+11800dup
XM_017006023.1:c.327+11800dup	XP_016861512.1:n.327+11800dup
XM_017006024.2:c.327+11800dup	XP_016861513.1:n.327+11800dup
XM_017006025.1:c.-2674dup	XP_016861514.1:n.-2674dup
NM_001144382.2:c.327+11800dup MANE Select	NP_001137854.1:n.327+11800dup