Canonical Allele Identifier: CA649690819
Gene: PLCXD3 HGNC NCBI

Linked Data

COSMIC: COSN15618706
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41475672G>T , CM000667.2:g.41475672G>T GRCh38
NC_000005.9:g.41475774G>T , CM000667.1:g.41475774G>T GRCh37
NC_000005.8:g.41511531G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377801.8:c.103+34752C>A MANE Select ENSP00000367032.3:n.103+34752C>A
ENST00000328457.5:c.103+34752C>A ENSP00000333751.3:n.103+34752C>A
ENST00000377801.7:c.103+34752C>A ENSP00000367032.3:n.103+34752C>A
NM_001005473.2:c.103+34752C>A NP_001005473.1:n.103+34752C>A
NM_001005473.3:c.103+34752C>A MANE Select NP_001005473.1:n.103+34752C>A
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