Canonical Allele Identifier: CA311224932

Gene: PLCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8684870del , CM000682.2:g.8684870del	GRCh38
NC_000020.10:g.8665517del , CM000682.1:g.8665517del	GRCh37
NC_000020.9:g.8613517del	NCBI36
NG_028168.1:g.557222del

Transcript Alleles

HGVS	Amino-acid Change
NM_015192.4:c.863-62del MANE Select	NP_056007.1:n.863-62del
ENST00000338037.11:c.863-62del MANE Select	ENSP00000338185.6:n.863-62del
NM_015192.3:c.863-62del	NP_056007.1:n.863-62del
NM_182734.2:c.863-62del	NP_877398.1:n.863-62del
NM_182734.3:c.863-62del	NP_877398.1:n.863-62del
ENST00000338037.10:c.863-62del	ENSP00000338185.6:n.863-62del
ENST00000378637.6:c.863-62del	ENSP00000367904.2:n.863-62del
ENST00000378641.7:c.863-62del	ENSP00000367908.3:n.863-62del
ENST00000487210.5:c.85-62del
ENST00000612075.4:c.623-62del	ENSP00000479997.1:n.623-62del
ENST00000617005.4:c.623-62del	ENSP00000477664.1:n.623-62del
ENST00000625874.2:c.560-62del	ENSP00000486301.1:n.560-62del
ENST00000626966.2:c.560-62del	ENSP00000487075.1:n.560-62del
ENST00000635830.1:n.934-62del
ENST00000636319.1:c.*306-62del	ENSP00000490455.1:n.*306-62del
ENST00000636825.1:n.727-62del
ENST00000637919.1:c.560-62del	ENSP00000490862.1:n.560-62del
XM_011529199.1:c.863-62del	XP_011527501.1:n.863-62del
XM_011529200.1:c.647-62del	XP_011527502.1:n.647-62del
XM_011529201.1:c.560-62del	XP_011527503.1:n.560-62del
XM_011529202.1:c.863-62del	XP_011527504.1:n.863-62del