Canonical Allele Identifier: CA2838221041

Gene: PLD5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.242437169C>T , CM000663.2:g.242437169C>T	GRCh38
NC_000001.10:g.242600471C>T , CM000663.1:g.242600471C>T	GRCh37
NC_000001.9:g.240667094C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536534.7:c.189+86919G>A MANE Select	ENSP00000440896.1:n.189+86919G>A
ENST00000314833.10:c.3+12185G>A	ENSP00000314748.6:n.3+12185G>A
ENST00000366545.5:c.189+86919G>A	ENSP00000355503.4:n.189+86919G>A
ENST00000427495.5:c.3+12185G>A	ENSP00000401285.1:n.3+12185G>A
ENST00000442594.6:c.189+86919G>A	ENSP00000414188.3:n.189+86919G>A
ENST00000459864.1:c.3+12185G>A	ENSP00000438191.1:n.3+12185G>A
ENST00000467561.5:c.189+86919G>A	ENSP00000440132.1:n.189+86919G>A
ENST00000536534.6:c.189+86919G>A	ENSP00000440896.1:n.189+86919G>A
NM_001195811.1:c.3+12185G>A	NP_001182740.1:n.3+12185G>A
NM_001195812.1:c.-274+12185G>A	NP_001182741.1:n.-274+12185G>A
NM_152666.2:c.189+86919G>A	NP_689879.2:n.189+86919G>A
XM_006711752.1:c.189+86919G>A	XP_006711815.1:n.189+86919G>A
XM_011544115.1:c.-84-88927G>A	XP_011542417.1:n.-84-88927G>A
XM_011544116.1:c.-84-88927G>A	XP_011542418.1:n.-84-88927G>A
XM_011544118.1:c.-95+86919G>A	XP_011542420.1:n.-95+86919G>A
NM_001320272.1:c.-95+86919G>A	NP_001307201.1:n.-95+86919G>A
XM_006711752.3:c.189+86919G>A	XP_006711815.1:n.189+86919G>A
XM_011544115.2:c.-84-88927G>A	XP_011542417.1:n.-84-88927G>A
XM_011544116.2:c.-84-88927G>A	XP_011542418.1:n.-84-88927G>A
XM_011544120.2:c.-411+86919G>A	XP_011542422.1:n.-411+86919G>A
XM_017000567.2:c.-95+86919G>A	XP_016856056.1:n.-95+86919G>A
XM_017000568.2:c.-95+12185G>A	XP_016856057.1:n.-95+12185G>A
XM_017000569.1:c.-418+12185G>A	XP_016856058.1:n.-418+12185G>A
NM_001195812.2:c.-274+12185G>A	NP_001182741.1:n.-274+12185G>A
NM_001320272.2:c.-95+86919G>A	NP_001307201.1:n.-95+86919G>A
NM_001372062.1:c.189+86919G>A MANE Select	NP_001358991.1:n.189+86919G>A
NM_001195811.2:c.3+12185G>A	NP_001182740.1:n.3+12185G>A