Canonical Allele Identifier: CA1928867256

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94032007C= , CM000672.2:g.94032007C=	GRCh38
NC_000010.10:g.95791764C= , CM000672.1:g.95791764C=	GRCh37
NC_000010.9:g.95781754C=	NCBI36
NG_015799.1:g.43019C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685253.1:c.961C=	ENSP00000509405.1:p.Arg321=
ENST00000686954.1:c.961C=	ENSP00000508416.1:p.Arg321=
ENST00000689233.1:n.1291C=
ENST00000689699.1:n.1291C=
ENST00000692286.1:c.961C=	ENSP00000509490.1:p.Arg321=
ENST00000692396.1:c.961C=	ENSP00000508605.1:p.Arg321=
ENST00000371380.8:c.961C= MANE Select	ENSP00000360431.2:p.Arg321=
ENST00000675487.1:c.961C=	ENSP00000502340.1:p.Arg321=
ENST00000675718.1:c.32C=
ENST00000260766.7:c.961C=	ENSP00000260766.3:p.Arg321=
ENST00000371380.7:c.961C=	ENSP00000360431.2:p.Arg321=
NM_001288989.1:c.961C=	NP_001275918.1:p.Arg321=
NM_016341.3:c.961C=	NP_057425.3:p.Arg321=
XM_006717885.2:c.961C=	XP_006717948.1:p.Arg321=
XM_006717886.2:c.961C=	XP_006717949.1:p.Arg321=
XM_006717888.2:c.961C=	XP_006717951.1:p.Arg321=
XM_006717889.2:c.961C=	XP_006717952.1:p.Arg321=
XM_011539849.1:c.961C=	XP_011538151.1:p.Arg321=
XM_011539851.1:c.961C=	XP_011538153.1:p.Arg321=
XM_011539852.1:c.961C=	XP_011538154.1:p.Arg321=
XM_006717885.4:c.961C=	XP_006717948.1:p.Arg321=
XM_006717888.4:c.961C=	XP_006717951.1:p.Arg321=
XM_006717889.4:c.961C=	XP_006717952.1:p.Arg321=
XM_011539849.3:c.961C=	XP_011538151.1:p.Arg321=
XM_011539851.3:c.961C=	XP_011538153.1:p.Arg321=
XM_011539852.3:c.961C=	XP_011538154.1:p.Arg321=
XM_017016310.2:c.961C=	XP_016871799.1:p.Arg321=
XM_017016311.2:c.961C=	XP_016871800.1:p.Arg321=
NM_001288989.2:c.961C=	NP_001275918.1:p.Arg321=
NM_016341.4:c.961C= MANE Select	NP_057425.3:p.Arg321=