Canonical Allele Identifier: CA1319566999

Gene: PLCL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.198098145G= , CM000664.2:g.198098145G=	GRCh38
NC_000002.11:g.198962869G= , CM000664.1:g.198962869G=	GRCh37
NC_000002.10:g.198671114G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000428675.6:c.2920-3140G= MANE Select	ENSP00000402861.1:n.2920-3140G=
ENST00000428675.5:c.2920-3140G=	ENSP00000402861.1:n.2920-3140G=
ENST00000435320.1:c.*2692-3140G=	ENSP00000410488.1:n.*2692-3140G=
ENST00000437704.3:c.2689-3140G=	ENSP00000414138.3:n.2689-3140G=
ENST00000487695.6:c.2698-3140G=	ENSP00000457588.1:n.2698-3140G=
NM_006226.3:c.2920-3140G=	NP_006217.3:n.2920-3140G=
XM_005246643.2:c.2698-3140G=	XP_005246700.1:n.2698-3140G=
XM_005246644.2:c.2683-3140G=	XP_005246701.1:n.2683-3140G=
XM_011511351.1:c.2683-3140G=	XP_011509653.1:n.2683-3140G=
XM_005246643.4:c.2698-3140G=	XP_005246700.1:n.2698-3140G=
XM_005246644.4:c.2683-3140G=	XP_005246701.1:n.2683-3140G=
XM_011511351.2:c.2683-3140G=	XP_011509653.1:n.2683-3140G=
XM_017004339.2:c.2683-3140G=	XP_016859828.1:n.2683-3140G=
XM_017004340.2:c.2626-3140G=	XP_016859829.1:n.2626-3140G=
NM_006226.4:c.2920-3140G= MANE Select	NP_006217.3:n.2920-3140G=