Canonical Allele Identifier: CA2202049768

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114529G= , CM000678.2:g.2114529G=	GRCh38
NC_000016.9:g.2164530G= , CM000678.1:g.2164530G=	GRCh37
NC_000016.8:g.2104531G=	NCBI36
NG_008617.1:g.26370C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2494C= MANE Select	ENSP00000262304.4:p.Arg832=
ENST00000262304.8:c.2494C=	ENSP00000262304.4:p.Arg832=
ENST00000423118.5:c.2494C=	ENSP00000399501.1:p.Arg832=
ENST00000488185.2:c.472+2960C=
ENST00000568591.5:c.1425C=	ENSP00000457162.1:n.1425C=
NM_000296.3:c.2494C=	NP_000287.3:p.Arg832=
NM_001009944.2:c.2494C=	NP_001009944.2:p.Arg832=
XM_011522525.1:c.2548C=	XP_011520827.1:p.Arg850=
XM_011522526.1:c.2548C=	XP_011520828.1:p.Arg850=
XM_011522527.1:c.2548C=	XP_011520829.1:p.Arg850=
XM_011522528.1:c.2548C=	XP_011520830.1:p.Arg850=
XM_011522529.1:c.2548C=	XP_011520831.1:p.Arg850=
XM_011522530.1:c.2494C=	XP_011520832.1:p.Arg832=
XM_011522531.1:c.2476C=	XP_011520833.1:p.Arg826=
XM_011522532.1:c.2422C=	XP_011520834.1:p.Arg808=
XM_011522533.1:c.2341C=	XP_011520835.1:p.Arg781=
XM_011522534.1:c.2284C=	XP_011520836.1:p.Arg762=
XM_011522535.1:c.370C=	XP_011520837.1:p.Arg124=
XM_011522536.1:c.2548C=	XP_011520838.1:p.Arg850=
XR_932867.1:n.2563C=
XR_932868.1:n.2563C=
XR_932869.1:n.2563C=
XR_932870.1:n.2563C=
XM_005255370.3:c.-556C=	XP_005255427.1:n.-556C=
XM_011522528.3:c.2548C=	XP_011520830.1:p.Arg850=
XM_011522529.2:c.2548C=	XP_011520831.1:p.Arg850=
XM_024450298.1:c.2494C=	XP_024306066.1:p.Arg832=
XM_024450299.1:c.2422C=	XP_024306067.1:p.Arg808=
XM_024450300.1:c.2284C=	XP_024306068.1:p.Arg762=
XM_024450301.1:c.370C=	XP_024306069.1:p.Arg124=
NM_000296.4:c.2494C=	NP_000287.4:p.Arg832=
NM_001009944.3:c.2494C= MANE Select	NP_001009944.3:p.Arg832=