Canonical Allele Identifier: CA1319541855
Gene: PLCL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198049304_198049305delinsTA , CM000664.2:g.198049304_198049305delinsTA GRCh38
NC_000002.11:g.198914028_198914029delinsTA , CM000664.1:g.198914028_198914029delinsTA GRCh37
NC_000002.10:g.198622273_198622274delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000428675.6:c.241-34454_241-34453delinsTA MANE Select ENSP00000402861.1:n.241-34454_241-34453delinsTA
ENST00000428675.5:c.241-34454_241-34453delinsTA ENSP00000402861.1:n.241-34454_241-34453delinsTA
ENST00000435320.1:c.*13-34454_*13-34453delinsTA ENSP00000410488.1:n.*13-34454_*13-34453delinsTA
ENST00000487695.6:c.19-34454_19-34453delinsTA ENSP00000457588.1:n.19-34454_19-34453delinsTA
NM_006226.3:c.241-34454_241-34453delinsTA NP_006217.3:n.241-34454_241-34453delinsTA
XM_005246643.2:c.19-34454_19-34453delinsTA XP_005246700.1:n.19-34454_19-34453delinsTA
XM_011511351.1:c.4-34454_4-34453delinsTA XP_011509653.1:n.4-34454_4-34453delinsTA
XM_005246643.4:c.19-34454_19-34453delinsTA XP_005246700.1:n.19-34454_19-34453delinsTA
XM_011511351.2:c.4-34454_4-34453delinsTA XP_011509653.1:n.4-34454_4-34453delinsTA
XM_017004339.2:c.4-34454_4-34453delinsTA XP_016859828.1:n.4-34454_4-34453delinsTA
XM_017004340.2:c.-54-34454_-54-34453delinsTA XP_016859829.1:n.-54-34454_-54-34453delinsTA
NM_006226.4:c.241-34454_241-34453delinsTA MANE Select NP_006217.3:n.241-34454_241-34453delinsTA