Canonical Allele Identifier: CA11428038

Gene: PLD1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171724845C>T , CM000665.2:g.171724845C>T	GRCh38
NC_000003.11:g.171442635C>T , CM000665.1:g.171442635C>T	GRCh37
NC_000003.10:g.172925329C>T	NCBI36
NG_029851.1:g.90650G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002662.5:c.666-57G>A MANE Select	NP_002653.1:n.666-57G>A
ENST00000351298.9:c.666-57G>A MANE Select	ENSP00000342793.4:n.666-57G>A
NM_001130081.2:c.666-57G>A	NP_001123553.1:n.666-57G>A
NM_001130081.3:c.666-57G>A	NP_001123553.1:n.666-57G>A
NM_002662.4:c.666-57G>A	NP_002653.1:n.666-57G>A
ENST00000351298.8:c.666-57G>A	ENSP00000342793.4:n.666-57G>A
ENST00000356327.9:c.666-57G>A	ENSP00000348681.5:n.666-57G>A
ENST00000475273.6:n.547-57G>A
ENST00000498278.5:n.736-57G>A
XM_005247533.1:c.666-57G>A	XP_005247590.1:n.666-57G>A
XM_005247533.2:c.666-57G>A	XP_005247590.1:n.666-57G>A
XM_005247534.1:c.666-57G>A	XP_005247591.1:n.666-57G>A
XM_005247534.2:c.666-57G>A	XP_005247591.1:n.666-57G>A
XM_011512897.1:c.666-57G>A	XP_011511199.1:n.666-57G>A
XM_011512898.1:c.666-57G>A	XP_011511200.1:n.666-57G>A
XM_017006623.2:c.666-57G>A	XP_016862112.1:n.666-57G>A
XR_001740174.1:n.862-57G>A
XR_001740175.1:n.862-57G>A
XR_924146.1:n.862-57G>A