Canonical Allele Identifier: CA649690852

Gene: PLCXD3

Linked Data

• COSMIC: COSN15625881

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41475694G>A , CM000667.2:g.41475694G>A	GRCh38
NC_000005.9:g.41475796G>A , CM000667.1:g.41475796G>A	GRCh37
NC_000005.8:g.41511553G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377801.8:c.103+34730C>T MANE Select	ENSP00000367032.3:n.103+34730C>T
ENST00000328457.5:c.103+34730C>T	ENSP00000333751.3:n.103+34730C>T
ENST00000377801.7:c.103+34730C>T	ENSP00000367032.3:n.103+34730C>T
NM_001005473.2:c.103+34730C>T	NP_001005473.1:n.103+34730C>T
NM_001005473.3:c.103+34730C>T MANE Select	NP_001005473.1:n.103+34730C>T