Canonical Allele Identifier: CA2335950073

Gene: PLD3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40371695T= , CM000681.2:g.40371695T=	GRCh38
NC_000019.9:g.40877602T= , CM000681.1:g.40877602T=	GRCh37
NC_000019.8:g.45569442T=	NCBI36
NG_034098.1:g.28271T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000493006.2:n.1582T=
ENST00000700616.1:c.701T=	ENSP00000515107.1:p.Met234=
ENST00000700617.1:c.701T=	ENSP00000515108.1:p.Met234=
ENST00000700618.1:c.701T=	ENSP00000515109.1:p.Met234=
ENST00000700619.1:c.701T=	ENSP00000515110.1:p.Met234=
ENST00000700620.1:c.701T=	ENSP00000515111.1:p.Met234=
ENST00000700621.1:c.701T=	ENSP00000515112.1:p.Met234=
ENST00000700622.1:n.851T=
ENST00000700623.1:c.701T=	ENSP00000515113.1:p.Met234=
ENST00000700624.1:c.635T=	ENSP00000515114.2:p.Met212=
ENST00000700625.1:c.701T=	ENSP00000515115.1:p.Met234=
ENST00000700626.1:c.701T=	ENSP00000515116.1:p.Met234=
ENST00000700628.1:c.701T=	ENSP00000515117.1:p.Met234=
ENST00000700630.1:c.701T=	ENSP00000515118.1:p.Met234=
ENST00000700631.1:c.701T=	ENSP00000515119.1:p.Met234=
ENST00000700632.1:c.701T=	ENSP00000515120.1:p.Met234=
ENST00000700633.1:c.701T=	ENSP00000515121.1:p.Met234=
ENST00000700634.1:c.701T=	ENSP00000515122.1:p.Met234=
ENST00000700635.1:n.887T=
ENST00000700636.1:n.887T=
ENST00000700637.1:c.701T=	ENSP00000515123.1:p.Met234=
ENST00000700638.1:c.623T=	ENSP00000515124.1:p.Met208=
ENST00000700639.1:n.191T=
ENST00000409735.9:c.701T= MANE Select	ENSP00000386938.3:p.Met234=
ENST00000356508.9:c.701T=	ENSP00000348901.5:p.Met234=
ENST00000409281.5:c.701T=	ENSP00000387022.1:p.Met234=
ENST00000409419.5:c.701T=	ENSP00000386293.1:p.Met234=
ENST00000409587.5:c.701T=	ENSP00000387050.1:p.Met234=
ENST00000409735.8:c.701T=	ENSP00000386938.3:p.Met234=
ENST00000475983.1:n.219T=
ENST00000492243.1:c.587T=
NM_001031696.3:c.701T=	NP_001026866.1:p.Met234=
NM_001291311.1:c.701T=	NP_001278240.1:p.Met234=
NM_012268.3:c.701T=	NP_036400.2:p.Met234=
XM_005258704.1:c.701T=	XP_005258761.1:p.Met234=
XM_005258705.2:c.701T=	XP_005258762.1:p.Met234=
XM_005258707.3:c.701T=	XP_005258764.1:p.Met234=
XM_005258708.2:c.701T=	XP_005258765.1:p.Met234=
XM_005258709.3:c.701T=	XP_005258766.1:p.Met234=
XM_005258710.3:c.701T=	XP_005258767.1:p.Met234=
XM_006723122.1:c.701T=	XP_006723185.1:p.Met234=
XM_011526692.1:c.701T=	XP_011524994.1:p.Met234=
XM_011526693.1:c.701T=	XP_011524995.1:p.Met234=
XM_005258704.2:c.701T=	XP_005258761.1:p.Met234=
XM_005258707.4:c.701T=	XP_005258764.1:p.Met234=
XM_005258708.4:c.701T=	XP_005258765.1:p.Met234=
XM_005258709.4:c.701T=	XP_005258766.1:p.Met234=
XM_005258710.5:c.701T=	XP_005258767.1:p.Met234=
XM_017026546.1:c.701T=	XP_016882035.1:p.Met234=
XM_017026548.1:c.701T=	XP_016882037.1:p.Met234=
XM_017026549.1:c.701T=	XP_016882038.1:p.Met234=
XM_024451438.1:c.701T=	XP_024307206.1:p.Met234=
NM_012268.4:c.701T= MANE Select	NP_036400.2:p.Met234=
NM_001031696.4:c.701T=	NP_001026866.1:p.Met234=
NM_001291311.2:c.701T=	NP_001278240.1:p.Met234=