Canonical Allele Identifier: CA897110263

Gene: PLCXD2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111704282G>A , CM000665.2:g.111704282G>A	GRCh38
NC_000003.11:g.111423129G>A , CM000665.1:g.111423129G>A	GRCh37
NC_000003.10:g.112905819G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636933.2:c.164-3644G>A MANE Select	ENSP00000490816.1:n.164-3644G>A
ENST00000477665.2:c.164-3644G>A	ENSP00000420686.1:n.164-3644G>A
ENST00000636933.1:c.164-3644G>A	ENSP00000490816.1:n.164-3644G>A
ENST00000393934.7:c.164-3644G>A	ENSP00000377511.3:n.164-3644G>A
ENST00000468174.1:c.-107-3644G>A	ENSP00000417436.1:n.-107-3644G>A
ENST00000477665.1:c.164-3644G>A	ENSP00000420686.1:n.164-3644G>A
NM_001185106.1:c.164-3644G>A	NP_001172035.1:n.164-3644G>A
NM_153268.3:c.164-3644G>A	NP_695000.1:n.164-3644G>A