Canonical Allele Identifier: CA11468289

Gene: PLCL2

Linked Data

• dbSNP Id: rs4452313
• gnomAD v2: 3-17047032-A-T
• gnomAD v3: 3-17005540-A-T
• gnomAD v4: 3-17005540-A-T
• MyVariant Identifiers: chr3:g.17047032A>T (hg19) ; chr3:g.17005540A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.17005540A>T , CM000665.2:g.17005540A>T	GRCh38
NC_000003.11:g.17047032A>T , CM000665.1:g.17047032A>T	GRCh37
NC_000003.10:g.17022036A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615277.5:c.328-4134A>T MANE Select	ENSP00000478458.1:n.328-4134A>T
ENST00000432376.5:c.-51-4134A>T	ENSP00000412836.1:n.-51-4134A>T
ENST00000460467.1:n.439-4134A>T
ENST00000615277.4:c.328-4134A>T	ENSP00000478458.1:n.328-4134A>T
NM_001144382.1:c.328-4134A>T	NP_001137854.1:n.328-4134A>T
NM_015184.5:c.-51-4134A>T	NP_055999.2:n.-51-4134A>T
XM_006713073.2:c.13-4134A>T	XP_006713136.1:n.13-4134A>T
XM_006713073.3:c.13-4134A>T	XP_006713136.1:n.13-4134A>T
XM_017006022.2:c.328-4134A>T	XP_016861511.1:n.328-4134A>T
XM_017006023.1:c.328-4134A>T	XP_016861512.1:n.328-4134A>T
XM_017006024.2:c.328-4134A>T	XP_016861513.1:n.328-4134A>T
XM_017006025.1:c.-51-4134A>T	XP_016861514.1:n.-51-4134A>T
NM_001144382.2:c.328-4134A>T MANE Select	NP_001137854.1:n.328-4134A>T