Canonical Allele Identifier: CA2349026935

Gene: PLCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737042G= , CM000682.2:g.8737042G=	GRCh38
NC_000020.10:g.8717689G= , CM000682.1:g.8717689G=	GRCh37
NC_000020.9:g.8665689G=	NCBI36
NG_028168.1:g.609394G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2058G= MANE Select	ENSP00000338185.6:p.Gln686=
ENST00000635830.1:n.2129G=
ENST00000636825.1:n.1922G=
ENST00000637919.1:c.1755G=	ENSP00000490862.1:p.Gln585=
ENST00000338037.10:c.2058G=	ENSP00000338185.6:p.Gln686=
ENST00000378637.6:c.2058G=	ENSP00000367904.2:p.Gln686=
ENST00000378641.7:c.2058G=	ENSP00000367908.3:p.Gln686=
ENST00000439627.2:c.15G=	ENSP00000391162.1:p.Gln5=
ENST00000487210.5:c.1280G=
ENST00000494924.2:n.1210G=
ENST00000612075.4:c.1818G=	ENSP00000479997.1:p.Gln606=
ENST00000617005.4:c.1818G=	ENSP00000477664.1:p.Gln606=
ENST00000625874.2:c.1755G=	ENSP00000486301.1:p.Gln585=
ENST00000626966.2:c.1755G=	ENSP00000487075.1:p.Gln585=
NM_015192.3:c.2058G=	NP_056007.1:p.Gln686=
NM_182734.2:c.2058G=	NP_877398.1:p.Gln686=
XM_011529199.1:c.2058G=	XP_011527501.1:p.Gln686=
XM_011529200.1:c.1842G=	XP_011527502.1:p.Gln614=
XM_011529201.1:c.1755G=	XP_011527503.1:p.Gln585=
XM_011529203.1:c.285G=	XP_011527505.1:p.Gln95=
NM_015192.4:c.2058G= MANE Select	NP_056007.1:p.Gln686=
NM_182734.3:c.2058G=	NP_877398.1:p.Gln686=