Canonical Allele Identifier: CA2349027081

Gene: PLCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737499_8737503delinsCAAAG , CM000682.2:g.8737499_8737503delinsCAAAG	GRCh38
NC_000020.10:g.8718146_8718150delinsCAAAG , CM000682.1:g.8718146_8718150delinsCAAAG	GRCh37
NC_000020.9:g.8666146_8666150delinsCAAAG	NCBI36
NG_028168.1:g.609851_609855delinsCAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2208+307_2208+311delinsCAAAG MANE Select	ENSP00000338185.6:n.2208+307_2208+311delinsCAAAG
ENST00000635830.1:n.2279+307_2279+311delinsCAAAG
ENST00000636825.1:n.2072+307_2072+311delinsCAAAG
ENST00000637919.1:c.1905+307_1905+311delinsCAAAG	ENSP00000490862.1:n.1905+307_1905+311delinsCAAAG
ENST00000338037.10:c.2208+307_2208+311delinsCAAAG	ENSP00000338185.6:n.2208+307_2208+311delinsCAAAG
ENST00000378637.6:c.2208+307_2208+311delinsCAAAG	ENSP00000367904.2:n.2208+307_2208+311delinsCAAAG
ENST00000378641.7:c.2208+307_2208+311delinsCAAAG	ENSP00000367908.3:n.2208+307_2208+311delinsCAAAG
ENST00000439627.2:c.165+307_165+311delinsCAAAG	ENSP00000391162.1:n.165+307_165+311delinsCAAAG
ENST00000487210.5:c.1430+307_1430+311delinsCAAAG
ENST00000494924.2:n.1360+307_1360+311delinsCAAAG
ENST00000612075.4:c.1968+307_1968+311delinsCAAAG	ENSP00000479997.1:n.1968+307_1968+311delinsCAAAG
ENST00000617005.4:c.1968+307_1968+311delinsCAAAG	ENSP00000477664.1:n.1968+307_1968+311delinsCAAAG
ENST00000625874.2:c.1905+307_1905+311delinsCAAAG	ENSP00000486301.1:n.1905+307_1905+311delinsCAAAG
ENST00000626966.2:c.1905+307_1905+311delinsCAAAG	ENSP00000487075.1:n.1905+307_1905+311delinsCAAAG
NM_015192.3:c.2208+307_2208+311delinsCAAAG	NP_056007.1:n.2208+307_2208+311delinsCAAAG
NM_182734.2:c.2208+307_2208+311delinsCAAAG	NP_877398.1:n.2208+307_2208+311delinsCAAAG
XM_011529199.1:c.2208+307_2208+311delinsCAAAG	XP_011527501.1:n.2208+307_2208+311delinsCAAAG
XM_011529200.1:c.1992+307_1992+311delinsCAAAG	XP_011527502.1:n.1992+307_1992+311delinsCAAAG
XM_011529201.1:c.1905+307_1905+311delinsCAAAG	XP_011527503.1:n.1905+307_1905+311delinsCAAAG
XM_011529203.1:c.435+307_435+311delinsCAAAG	XP_011527505.1:n.435+307_435+311delinsCAAAG
NM_015192.4:c.2208+307_2208+311delinsCAAAG MANE Select	NP_056007.1:n.2208+307_2208+311delinsCAAAG
NM_182734.3:c.2208+307_2208+311delinsCAAAG	NP_877398.1:n.2208+307_2208+311delinsCAAAG