Canonical Allele Identifier: CA1541659149
Gene: PLCXD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41475675T= , CM000667.2:g.41475675T= GRCh38
NC_000005.9:g.41475777T= , CM000667.1:g.41475777T= GRCh37
NC_000005.8:g.41511534T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377801.8:c.103+34749A= MANE Select ENSP00000367032.3:n.103+34749A=
ENST00000328457.5:c.103+34749A= ENSP00000333751.3:n.103+34749A=
ENST00000377801.7:c.103+34749A= ENSP00000367032.3:n.103+34749A=
NM_001005473.2:c.103+34749A= NP_001005473.1:n.103+34749A=
NM_001005473.3:c.103+34749A= MANE Select NP_001005473.1:n.103+34749A=
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