Canonical Allele Identifier: CA11291953

Gene: PLCL1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197835492G>A , CM000664.2:g.197835492G>A	GRCh38
NC_000002.11:g.198700216G>A , CM000664.1:g.198700216G>A	GRCh37
NC_000002.10:g.198408461G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428675.6:c.240+30153G>A MANE Select	ENSP00000402861.1:n.240+30153G>A
ENST00000428675.5:c.240+30153G>A	ENSP00000402861.1:n.240+30153G>A
ENST00000435320.1:c.240+30153G>A	ENSP00000410488.1:n.240+30153G>A
ENST00000487695.6:c.18+25170G>A	ENSP00000457588.1:n.18+25170G>A
NM_006226.3:c.240+30153G>A	NP_006217.3:n.240+30153G>A
XM_005246643.2:c.18+25170G>A	XP_005246700.1:n.18+25170G>A
XM_011511351.1:c.-55+30153G>A	XP_011509653.1:n.-55+30153G>A
XM_005246643.4:c.18+25170G>A	XP_005246700.1:n.18+25170G>A
XM_011511351.2:c.-55+30153G>A	XP_011509653.1:n.-55+30153G>A
NM_006226.4:c.240+30153G>A MANE Select	NP_006217.3:n.240+30153G>A