Canonical Allele Identifier: CA763077139

Gene: PLCL1

Linked Data

• dbSNP Id: rs1219068184
• gnomAD v3: 2-198016900-T-C
• gnomAD v4: 2-198016900-T-C
• MyVariant Identifiers: chr2:g.198881624T>C (hg19) ; chr2:g.198016900T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.198016900T>C , CM000664.2:g.198016900T>C	GRCh38
NC_000002.11:g.198881624T>C , CM000664.1:g.198881624T>C	GRCh37
NC_000002.10:g.198589869T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000428675.6:c.241-66858T>C MANE Select	ENSP00000402861.1:n.241-66858T>C
ENST00000428675.5:c.241-66858T>C	ENSP00000402861.1:n.241-66858T>C
ENST00000435320.1:c.*12+14892T>C	ENSP00000410488.1:n.*12+14892T>C
ENST00000487695.6:c.19-66858T>C	ENSP00000457588.1:n.19-66858T>C
NM_006226.3:c.241-66858T>C	NP_006217.3:n.241-66858T>C
XM_005246643.2:c.19-66858T>C	XP_005246700.1:n.19-66858T>C
XM_011511351.1:c.3+14892T>C	XP_011509653.1:n.3+14892T>C
XM_005246643.4:c.19-66858T>C	XP_005246700.1:n.19-66858T>C
XM_011511351.2:c.3+14892T>C	XP_011509653.1:n.3+14892T>C
XM_017004339.2:c.3+14892T>C	XP_016859828.1:n.3+14892T>C
XM_017004340.2:c.-55+50199T>C	XP_016859829.1:n.-55+50199T>C
NM_006226.4:c.241-66858T>C MANE Select	NP_006217.3:n.241-66858T>C