Canonical Allele Identifier: CA63740513
Gene: PLCL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10497813

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198049348G>T , CM000664.2:g.198049348G>T GRCh38
NC_000002.11:g.198914072G>T , CM000664.1:g.198914072G>T GRCh37
NC_000002.10:g.198622317G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_006226.3:c.241-34410G>T VV NP_006217.3:p.=
XM_005246643.2:c.19-34410G>T XP_005246700.1:p.=
XM_011511351.1:c.4-34410G>T XP_011509653.1:p.=
XM_005246643.4:c.19-34410G>T
XM_011511351.2:c.4-34410G>T
XM_017004339.2:c.4-34410G>T XP_016859828.1:p.=
XM_017004340.2:c.-54-34410G>T XP_016859829.1:p.=
ENST00000428675.5:c.241-34410G>T ENSP00000402861.1:p.=
ENST00000435320.1:c.*13-34410G>T ENSP00000410488.1:p.=
ENST00000487695.6:c.19-34410G>T ENSP00000457588.1:p.=