Canonical Allele Identifier: CA63700273

Gene: PLCL1

Linked Data

• dbSNP Id: rs959831662
• MyVariant Identifiers: chr2:g.198881611C>A (hg19) ; chr2:g.198016887C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.198016887C>A , CM000664.2:g.198016887C>A	GRCh38
NC_000002.11:g.198881611C>A , CM000664.1:g.198881611C>A	GRCh37
NC_000002.10:g.198589856C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000428675.6:c.241-66871C>A MANE Select	ENSP00000402861.1:n.241-66871C>A
ENST00000428675.5:c.241-66871C>A	ENSP00000402861.1:n.241-66871C>A
ENST00000435320.1:c.*12+14879C>A	ENSP00000410488.1:n.*12+14879C>A
ENST00000487695.6:c.19-66871C>A	ENSP00000457588.1:n.19-66871C>A
NM_006226.3:c.241-66871C>A	NP_006217.3:n.241-66871C>A
XM_005246643.2:c.19-66871C>A	XP_005246700.1:n.19-66871C>A
XM_011511351.1:c.3+14879C>A	XP_011509653.1:n.3+14879C>A
XM_005246643.4:c.19-66871C>A	XP_005246700.1:n.19-66871C>A
XM_011511351.2:c.3+14879C>A	XP_011509653.1:n.3+14879C>A
XM_017004339.2:c.3+14879C>A	XP_016859828.1:n.3+14879C>A
XM_017004340.2:c.-55+50186C>A	XP_016859829.1:n.-55+50186C>A
NM_006226.4:c.241-66871C>A MANE Select	NP_006217.3:n.241-66871C>A