Canonical Allele Identifier: CA1541659142
Gene: PLCXD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41475664C= , CM000667.2:g.41475664C= GRCh38
NC_000005.9:g.41475766C= , CM000667.1:g.41475766C= GRCh37
NC_000005.8:g.41511523C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377801.8:c.103+34760G= MANE Select ENSP00000367032.3:n.103+34760G=
ENST00000328457.5:c.103+34760G= ENSP00000333751.3:n.103+34760G=
ENST00000377801.7:c.103+34760G= ENSP00000367032.3:n.103+34760G=
NM_001005473.2:c.103+34760G= NP_001005473.1:n.103+34760G=
NM_001005473.3:c.103+34760G= MANE Select NP_001005473.1:n.103+34760G=
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