Canonical Allele Identifier: CA1319541888

Gene: PLCL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.198049389T= , CM000664.2:g.198049389T=	GRCh38
NC_000002.11:g.198914113T= , CM000664.1:g.198914113T=	GRCh37
NC_000002.10:g.198622358T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000428675.6:c.241-34369T= MANE Select	ENSP00000402861.1:n.241-34369T=
ENST00000428675.5:c.241-34369T=	ENSP00000402861.1:n.241-34369T=
ENST00000435320.1:c.*13-34369T=	ENSP00000410488.1:n.*13-34369T=
ENST00000487695.6:c.19-34369T=	ENSP00000457588.1:n.19-34369T=
NM_006226.3:c.241-34369T=	NP_006217.3:n.241-34369T=
XM_005246643.2:c.19-34369T=	XP_005246700.1:n.19-34369T=
XM_011511351.1:c.4-34369T=	XP_011509653.1:n.4-34369T=
XM_005246643.4:c.19-34369T=	XP_005246700.1:n.19-34369T=
XM_011511351.2:c.4-34369T=	XP_011509653.1:n.4-34369T=
XM_017004339.2:c.4-34369T=	XP_016859828.1:n.4-34369T=
XM_017004340.2:c.-54-34369T=	XP_016859829.1:n.-54-34369T=
NM_006226.4:c.241-34369T= MANE Select	NP_006217.3:n.241-34369T=