Canonical Allele Identifier: CA734016072

Gene: PLCH2

Linked Data

• dbSNP Id: rs1428609011
• gnomAD v3: 1-2461197-CG-C
• gnomAD v4: 1-2461197-CG-C
• MyVariant Identifiers: chr1:g.2392637del (hg19) ; chr1:g.2461198del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2461200del , CM000663.2:g.2461200del	GRCh38
NC_000001.10:g.2392639del , CM000663.1:g.2392639del	GRCh37
NC_000001.9:g.2382499del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609981.5:c.116-17276del	ENSP00000476436.1:n.116-17276del
XM_011542449.1:c.365-17276del	XP_011540751.1:n.365-17276del
XM_011542450.1:c.365-17276del	XP_011540752.1:n.365-17276del
XM_011542452.1:c.31+17228del	XP_011540754.1:n.31+17228del
XM_011542454.1:c.365-17276del	XP_011540756.1:n.365-17276del
XM_011542455.1:c.116-17276del	XP_011540757.1:n.116-17276del
XM_011542456.1:c.116-17276del	XP_011540758.1:n.116-17276del
XM_011542457.1:c.365-17276del	XP_011540759.1:n.365-17276del
XM_011542459.1:c.365-17276del	XP_011540761.1:n.365-17276del
XM_011542460.1:c.365-17276del	XP_011540762.1:n.365-17276del
XR_946803.1:n.392-17276del
XM_017002870.1:c.410-17276del	XP_016858359.1:n.410-17276del
XM_017002872.1:c.410-17276del	XP_016858361.1:n.410-17276del
XM_017002873.1:c.410-17276del	XP_016858362.1:n.410-17276del
XM_017002874.1:c.410-17276del	XP_016858363.1:n.410-17276del
XM_024451058.1:c.386-17276del	XP_024306826.1:n.386-17276del
XM_024451059.1:c.410-17276del	XP_024306827.1:n.410-17276del
XM_024451060.1:c.116-17276del	XP_024306828.1:n.116-17276del
XM_024451061.1:c.116-17276del	XP_024306829.1:n.116-17276del
XM_024451062.1:c.410-17276del	XP_024306830.1:n.410-17276del
XM_024451063.1:c.410-17276del	XP_024306831.1:n.410-17276del
XM_024451064.1:c.410-17276del	XP_024306832.1:n.410-17276del