Canonical Allele Identifier: CA2202021099

Gene: PKD1 PKD1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2092501G= , CM000678.2:g.2092501G=	GRCh38
NC_000016.9:g.2142502G= , CM000678.1:g.2142502G=	GRCh37
NC_000016.8:g.2082503G=	NCBI36
NG_008617.1:g.50720C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.11248C= (PKD1) MANE Select	ENSP00000262304.4:p.Arg3750=
ENST00000262304.8:c.11248C= (PKD1)	ENSP00000262304.4:p.Arg3750=
ENST00000423118.5:c.11245C= (PKD1)	ENSP00000399501.1:p.Arg3749=
ENST00000485120.1:n.97C= (PKD1)
ENST00000487932.5:c.5810C= (PKD1)	ENSP00000457132.1:n.5810C=
ENST00000562425.1:c.361C= (PKD1)
ENST00000567355.1:n.411C= (PKD1)
NM_000296.3:c.11245C= (PKD1)	NP_000287.3:p.Arg3749=
NM_001009944.2:c.11248C= (PKD1)	NP_001009944.2:p.Arg3750=
XM_005255370.2:c.8203C= (PKD1)	XP_005255427.1:p.Arg2735=
XM_011522525.1:c.11326C= (PKD1)	XP_011520827.1:p.Arg3776=
XM_011522526.1:c.11323C= (PKD1)	XP_011520828.1:p.Arg3775=
XM_011522527.1:c.11308C= (PKD1)	XP_011520829.1:p.Arg3770=
XM_011522528.1:c.11302C= (PKD1)	XP_011520830.1:p.Arg3768=
XM_011522529.1:c.11299C= (PKD1)	XP_011520831.1:p.Arg3767=
XM_011522530.1:c.11272C= (PKD1)	XP_011520832.1:p.Arg3758=
XM_011522531.1:c.11254C= (PKD1)	XP_011520833.1:p.Arg3752=
XM_011522532.1:c.11200C= (PKD1)	XP_011520834.1:p.Arg3734=
XM_011522533.1:c.11119C= (PKD1)	XP_011520835.1:p.Arg3707=
XM_011522534.1:c.11062C= (PKD1)	XP_011520836.1:p.Arg3688=
XM_011522535.1:c.9148C= (PKD1)	XP_011520837.1:p.Arg3050=
XM_011522537.1:c.8326C= (PKD1)	XP_011520839.1:p.Arg2776=
XR_932867.1:n.11341C= (PKD1)
XR_932868.1:n.11110-313C= (PKD1)
XR_932869.1:n.11110-313C= (PKD1)
XR_932870.1:n.11201C= (PKD1)
XR_933000.1:n.90-388G= (PKD1-AS1)
XR_933001.1:n.180-388G= (PKD1-AS1)
XR_933002.1:n.89-388G= (PKD1-AS1)
XR_933003.1:n.89-388G= (PKD1-AS1)
NR_135175.1:n.180-388G= (PKD1-AS1)
XM_005255370.3:c.8203C= (PKD1)	XP_005255427.1:p.Arg2735=
XM_011522528.3:c.11302C= (PKD1)	XP_011520830.1:p.Arg3768=
XM_011522529.2:c.11299C= (PKD1)	XP_011520831.1:p.Arg3767=
XM_011522537.2:c.8326C= (PKD1)	XP_011520839.1:p.Arg2776=
XM_024450298.1:c.11368C= (PKD1)	XP_024306066.1:p.Arg3790=
XM_024450299.1:c.11296C= (PKD1)	XP_024306067.1:p.Arg3766=
XM_024450300.1:c.11158C= (PKD1)	XP_024306068.1:p.Arg3720=
XM_024450301.1:c.9244C= (PKD1)	XP_024306069.1:p.Arg3082=
NM_000296.4:c.11245C= (PKD1)	NP_000287.4:p.Arg3749=
NM_001009944.3:c.11248C= (PKD1) MANE Select	NP_001009944.3:p.Arg3750=