Canonical Allele Identifier: CA763098337
Gene: PLCL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197835492G>C , CM000664.2:g.197835492G>C GRCh38
NC_000002.11:g.198700216G>C , CM000664.1:g.198700216G>C GRCh37
NC_000002.10:g.198408461G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000428675.6:c.240+30153G>C MANE Select ENSP00000402861.1:n.240+30153G>C
ENST00000428675.5:c.240+30153G>C ENSP00000402861.1:n.240+30153G>C
ENST00000435320.1:c.240+30153G>C ENSP00000410488.1:n.240+30153G>C
ENST00000487695.6:c.18+25170G>C ENSP00000457588.1:n.18+25170G>C
NM_006226.3:c.240+30153G>C NP_006217.3:n.240+30153G>C
XM_005246643.2:c.18+25170G>C XP_005246700.1:n.18+25170G>C
XM_011511351.1:c.-55+30153G>C XP_011509653.1:n.-55+30153G>C
XM_005246643.4:c.18+25170G>C XP_005246700.1:n.18+25170G>C
XM_011511351.2:c.-55+30153G>C XP_011509653.1:n.-55+30153G>C
NM_006226.4:c.240+30153G>C MANE Select NP_006217.3:n.240+30153G>C
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