Canonical Allele Identifier: CA2202049789

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114562C= , CM000678.2:g.2114562C=	GRCh38
NC_000016.9:g.2164563C= , CM000678.1:g.2164563C=	GRCh37
NC_000016.8:g.2104564C=	NCBI36
NG_008617.1:g.26337G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2461G= MANE Select	ENSP00000262304.4:p.Val821=
ENST00000262304.8:c.2461G=	ENSP00000262304.4:p.Val821=
ENST00000423118.5:c.2461G=	ENSP00000399501.1:p.Val821=
ENST00000488185.2:c.472+2927G=
ENST00000568591.5:c.1392G=	ENSP00000457162.1:n.1392G=
NM_000296.3:c.2461G=	NP_000287.3:p.Val821=
NM_001009944.2:c.2461G=	NP_001009944.2:p.Val821=
XM_011522525.1:c.2515G=	XP_011520827.1:p.Val839=
XM_011522526.1:c.2515G=	XP_011520828.1:p.Val839=
XM_011522527.1:c.2515G=	XP_011520829.1:p.Val839=
XM_011522528.1:c.2515G=	XP_011520830.1:p.Val839=
XM_011522529.1:c.2515G=	XP_011520831.1:p.Val839=
XM_011522530.1:c.2461G=	XP_011520832.1:p.Val821=
XM_011522531.1:c.2443G=	XP_011520833.1:p.Val815=
XM_011522532.1:c.2389G=	XP_011520834.1:p.Val797=
XM_011522533.1:c.2308G=	XP_011520835.1:p.Val770=
XM_011522534.1:c.2251G=	XP_011520836.1:p.Val751=
XM_011522535.1:c.337G=	XP_011520837.1:p.Val113=
XM_011522536.1:c.2515G=	XP_011520838.1:p.Val839=
XR_932867.1:n.2530G=
XR_932868.1:n.2530G=
XR_932869.1:n.2530G=
XR_932870.1:n.2530G=
XM_005255370.3:c.-589G=	XP_005255427.1:n.-589G=
XM_011522528.3:c.2515G=	XP_011520830.1:p.Val839=
XM_011522529.2:c.2515G=	XP_011520831.1:p.Val839=
XM_024450298.1:c.2461G=	XP_024306066.1:p.Val821=
XM_024450299.1:c.2389G=	XP_024306067.1:p.Val797=
XM_024450300.1:c.2251G=	XP_024306068.1:p.Val751=
XM_024450301.1:c.337G=	XP_024306069.1:p.Val113=
NM_000296.4:c.2461G=	NP_000287.4:p.Val821=
NM_001009944.3:c.2461G= MANE Select	NP_001009944.3:p.Val821=