Canonical Allele Identifier: CA10758485

Gene: PLD5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.242313953G>A , CM000663.2:g.242313953G>A	GRCh38
NC_000001.10:g.242477255G>A , CM000663.1:g.242477255G>A	GRCh37
NC_000001.9:g.240543878G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536534.7:c.327-25423C>T MANE Select	ENSP00000440896.1:n.327-25423C>T
ENST00000314833.10:c.*3+34146C>T	ENSP00000314748.6:n.*3+34146C>T
ENST00000366545.5:c.*4-25423C>T	ENSP00000355503.4:n.*4-25423C>T
ENST00000427495.5:c.141-25423C>T	ENSP00000401285.1:n.141-25423C>T
ENST00000442594.6:c.327-25423C>T	ENSP00000414188.3:n.327-25423C>T
ENST00000459864.1:c.141-25423C>T	ENSP00000438191.1:n.141-25423C>T
ENST00000467561.5:c.327-25423C>T	ENSP00000440132.1:n.327-25423C>T
ENST00000536534.6:c.327-25423C>T	ENSP00000440896.1:n.327-25423C>T
NM_001195811.1:c.141-25423C>T	NP_001182740.1:n.141-25423C>T
NM_001195812.1:c.-130+34146C>T	NP_001182741.1:n.-130+34146C>T
NM_152666.2:c.327-25423C>T	NP_689879.2:n.327-25423C>T
XM_006711752.1:c.327-25423C>T	XP_006711815.1:n.327-25423C>T
XM_011544115.1:c.54-25423C>T	XP_011542417.1:n.54-25423C>T
XM_011544116.1:c.54-25423C>T	XP_011542418.1:n.54-25423C>T
XM_011544117.1:c.54-25423C>T	XP_011542419.1:n.54-25423C>T
XM_011544118.1:c.51-25423C>T	XP_011542420.1:n.51-25423C>T
NM_001320272.1:c.51-25423C>T	NP_001307201.1:n.51-25423C>T
XM_006711752.3:c.327-25423C>T	XP_006711815.1:n.327-25423C>T
XM_011544115.2:c.54-25423C>T	XP_011542417.1:n.54-25423C>T
XM_011544116.2:c.54-25423C>T	XP_011542418.1:n.54-25423C>T
XM_011544120.2:c.-273-25423C>T	XP_011542422.1:n.-273-25423C>T
XM_017000567.2:c.51-25423C>T	XP_016856056.1:n.51-25423C>T
XM_017000568.2:c.51-25423C>T	XP_016856057.1:n.51-25423C>T
XM_017000569.1:c.-273-25423C>T	XP_016856058.1:n.-273-25423C>T
XM_024453867.1:c.198-25423C>T	XP_024309635.1:n.198-25423C>T
NM_001195812.2:c.-130+34146C>T	NP_001182741.1:n.-130+34146C>T
NM_001320272.2:c.51-25423C>T	NP_001307201.1:n.51-25423C>T
NM_001372062.1:c.327-25423C>T MANE Select	NP_001358991.1:n.327-25423C>T
NM_001195811.2:c.141-25423C>T	NP_001182740.1:n.141-25423C>T