Canonical Allele Identifier: CA2202035157

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106585C= , CM000678.2:g.2106585C=	GRCh38
NC_000016.9:g.2156586C= , CM000678.1:g.2156586C=	GRCh37
NC_000016.8:g.2096587C=	NCBI36
NG_008617.1:g.34314G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7302G= MANE Select	ENSP00000262304.4:p.Arg2434=
ENST00000262304.8:c.7302G=	ENSP00000262304.4:p.Arg2434=
ENST00000415938.7:n.547G=
ENST00000423118.5:c.7302G=	ENSP00000399501.1:p.Arg2434=
ENST00000483558.5:n.361G=
ENST00000483731.5:n.1027G=
ENST00000486339.6:n.1048G=
ENST00000487932.5:c.1989G=	ENSP00000457132.1:p.Arg663=
ENST00000496574.6:n.1305G=
ENST00000565639.6:n.1010G=
ENST00000568591.5:c.2463G=	ENSP00000457162.1:n.2463G=
ENST00000569983.5:n.658G=
NM_000296.3:c.7302G=	NP_000287.3:p.Arg2434=
NM_001009944.2:c.7302G=	NP_001009944.2:p.Arg2434=
XM_005255370.2:c.4257G=	XP_005255427.1:p.Arg1419=
XM_011522525.1:c.7380G=	XP_011520827.1:p.Arg2460=
XM_011522526.1:c.7380G=	XP_011520828.1:p.Arg2460=
XM_011522527.1:c.7380G=	XP_011520829.1:p.Arg2460=
XM_011522528.1:c.7356G=	XP_011520830.1:p.Arg2452=
XM_011522529.1:c.7356G=	XP_011520831.1:p.Arg2452=
XM_011522530.1:c.7326G=	XP_011520832.1:p.Arg2442=
XM_011522531.1:c.7308G=	XP_011520833.1:p.Arg2436=
XM_011522532.1:c.7254G=	XP_011520834.1:p.Arg2418=
XM_011522533.1:c.7173G=	XP_011520835.1:p.Arg2391=
XM_011522534.1:c.7116G=	XP_011520836.1:p.Arg2372=
XM_011522535.1:c.5202G=	XP_011520837.1:p.Arg1734=
XM_011522536.1:c.7380G=	XP_011520838.1:p.Arg2460=
XM_011522537.1:c.4380G=	XP_011520839.1:p.Arg1460=
XR_932867.1:n.7395G=
XR_932868.1:n.7395G=
XR_932869.1:n.7395G=
XR_932870.1:n.7395G=
XM_005255370.3:c.4257G=	XP_005255427.1:p.Arg1419=
XM_011522528.3:c.7356G=	XP_011520830.1:p.Arg2452=
XM_011522529.2:c.7356G=	XP_011520831.1:p.Arg2452=
XM_011522537.2:c.4380G=	XP_011520839.1:p.Arg1460=
XM_024450298.1:c.7422G=	XP_024306066.1:p.Arg2474=
XM_024450299.1:c.7350G=	XP_024306067.1:p.Arg2450=
XM_024450300.1:c.7212G=	XP_024306068.1:p.Arg2404=
XM_024450301.1:c.5298G=	XP_024306069.1:p.Arg1766=
NM_000296.4:c.7302G=	NP_000287.4:p.Arg2434=
NM_001009944.3:c.7302G= MANE Select	NP_001009944.3:p.Arg2434=