Canonical Allele Identifier: CA470986559
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058308C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298551C>A , CM000672.2:g.94298551C>A GRCh38
NC_000010.10:g.96058308C>A , CM000672.1:g.96058308C>A GRCh37
NC_000010.9:g.96048298C>A NCBI36
NG_015799.1:g.309563C>A

Transcript Alleles

HGVS Amino-acid change
NM_001165979.2:c.4416C>A NP_001159451.1:p.Thr1472=
NM_001288989.1:c.5292C>A NP_001275918.1:p.Thr1764=
NM_016341.3:c.5340C>A NP_057425.3:p.Thr1780=
XM_006717885.2:c.5382C>A XP_006717948.1:p.Thr1794=
XM_006717886.2:c.5382C>A XP_006717949.1:p.Thr1794=
XM_006717888.2:c.5379C>A XP_006717951.1:p.Thr1793=
XM_006717889.2:c.5334C>A XP_006717952.1:p.Thr1778=
XM_006717890.1:c.4458C>A XP_006717953.1:p.Thr1486=
XM_011539849.1:c.5382C>A XP_011538151.1:p.Thr1794=
XM_011539850.1:c.4227C>A XP_011538152.1:p.Thr1409=
XM_006717885.4:c.5382C>A XP_006717948.1:p.Thr1794=
XM_006717888.4:c.5379C>A XP_006717951.1:p.Thr1793=
XM_006717889.4:c.5334C>A XP_006717952.1:p.Thr1778=
XM_006717890.3:c.4458C>A XP_006717953.1:p.Thr1486=
XM_011539849.3:c.5382C>A XP_011538151.1:p.Thr1794=
XM_011539850.3:c.4227C>A XP_011538152.1:p.Thr1409=
XM_017016310.2:c.5382C>A XP_016871799.1:p.Thr1794=
XM_017016311.2:c.5382C>A XP_016871800.1:p.Thr1794=
XM_017016312.2:c.4368C>A XP_016871801.1:p.Thr1456=
NM_001288989.2:c.5292C>A NP_001275918.1:p.Thr1764=
NM_016341.4:c.5340C>A MANE Select NP_057425.3:p.Thr1780=
ENST00000260766.7:c.5340C>A ENSP00000260766.3:p.Thr1780=
ENST00000371375.1:n.4416C>A ENSP00000360426.1:p.Thr1472=
ENST00000371380.7:c.5340C>A ENSP00000360431.2:p.Thr1780=
ENST00000371385.7:c.4416C>A ENSP00000360438.3:p.Thr1472=