Canonical Allele Identifier: CA2202035146

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106583C= , CM000678.2:g.2106583C=	GRCh38
NC_000016.9:g.2156584C= , CM000678.1:g.2156584C=	GRCh37
NC_000016.8:g.2096585C=	NCBI36
NG_008617.1:g.34316G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7304G= MANE Select	ENSP00000262304.4:p.Arg2435=
ENST00000262304.8:c.7304G=	ENSP00000262304.4:p.Arg2435=
ENST00000415938.7:n.549G=
ENST00000423118.5:c.7304G=	ENSP00000399501.1:p.Arg2435=
ENST00000483558.5:n.363G=
ENST00000483731.5:n.1029G=
ENST00000486339.6:n.1050G=
ENST00000487932.5:c.1991G=	ENSP00000457132.1:p.Arg664=
ENST00000496574.6:n.1307G=
ENST00000565639.6:n.1012G=
ENST00000568591.5:c.2465G=	ENSP00000457162.1:n.2465G=
ENST00000569983.5:n.660G=
NM_000296.3:c.7304G=	NP_000287.3:p.Arg2435=
NM_001009944.2:c.7304G=	NP_001009944.2:p.Arg2435=
XM_005255370.2:c.4259G=	XP_005255427.1:p.Arg1420=
XM_011522525.1:c.7382G=	XP_011520827.1:p.Arg2461=
XM_011522526.1:c.7382G=	XP_011520828.1:p.Arg2461=
XM_011522527.1:c.7382G=	XP_011520829.1:p.Arg2461=
XM_011522528.1:c.7358G=	XP_011520830.1:p.Arg2453=
XM_011522529.1:c.7358G=	XP_011520831.1:p.Arg2453=
XM_011522530.1:c.7328G=	XP_011520832.1:p.Arg2443=
XM_011522531.1:c.7310G=	XP_011520833.1:p.Arg2437=
XM_011522532.1:c.7256G=	XP_011520834.1:p.Arg2419=
XM_011522533.1:c.7175G=	XP_011520835.1:p.Arg2392=
XM_011522534.1:c.7118G=	XP_011520836.1:p.Arg2373=
XM_011522535.1:c.5204G=	XP_011520837.1:p.Arg1735=
XM_011522536.1:c.7382G=	XP_011520838.1:p.Arg2461=
XM_011522537.1:c.4382G=	XP_011520839.1:p.Arg1461=
XR_932867.1:n.7397G=
XR_932868.1:n.7397G=
XR_932869.1:n.7397G=
XR_932870.1:n.7397G=
XM_005255370.3:c.4259G=	XP_005255427.1:p.Arg1420=
XM_011522528.3:c.7358G=	XP_011520830.1:p.Arg2453=
XM_011522529.2:c.7358G=	XP_011520831.1:p.Arg2453=
XM_011522537.2:c.4382G=	XP_011520839.1:p.Arg1461=
XM_024450298.1:c.7424G=	XP_024306066.1:p.Arg2475=
XM_024450299.1:c.7352G=	XP_024306067.1:p.Arg2451=
XM_024450300.1:c.7214G=	XP_024306068.1:p.Arg2405=
XM_024450301.1:c.5300G=	XP_024306069.1:p.Arg1767=
NM_000296.4:c.7304G=	NP_000287.4:p.Arg2435=
NM_001009944.3:c.7304G= MANE Select	NP_001009944.3:p.Arg2435=