Canonical Allele Identifier: CA11237675
Gene: PLCL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1016883

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198016944G>A , CM000664.2:g.198016944G>A GRCh38
NC_000002.10:g.198589913G>A NCBI36
NC_000002.11:g.198881668G>A , CM000664.1:g.198881668G>A GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000428675.5:c.241-66814G>A ENSP00000402861.1:p.=
ENST00000435320.1:c.*12+14936G>A ENSP00000410488.1:p.=
ENST00000487695.6:c.19-66814G>A ENSP00000457588.1:p.=
NM_006226.3:c.241-66814G>A VV NP_006217.3:p.=
XM_005246643.2:c.19-66814G>A XP_005246700.1:p.=
XM_011511351.1:c.3+14936G>A XP_011509653.1:p.=
XM_005246643.4:c.19-66814G>A
XM_011511351.2:c.3+14936G>A
XM_017004339.2:c.3+14936G>A XP_016859828.1:p.=
XM_017004340.2:c.-55+50243G>A XP_016859829.1:p.=