Canonical Allele Identifier: CA2202046464

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2109732G= , CM000678.2:g.2109732G=	GRCh38
NC_000016.9:g.2159733G= , CM000678.1:g.2159733G=	GRCh37
NC_000016.8:g.2099734G=	NCBI36
NG_008617.1:g.31167C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.5435C= MANE Select	ENSP00000262304.4:p.Pro1812=
ENST00000262304.8:c.5435C=	ENSP00000262304.4:p.Pro1812=
ENST00000415938.7:n.310+2608C=
ENST00000423118.5:c.5435C=	ENSP00000399501.1:p.Pro1812=
ENST00000468674.5:n.431-382C=
ENST00000483024.1:c.233+2084C=
ENST00000483731.5:n.790+2608C=
ENST00000487932.5:c.122C=	ENSP00000457132.1:p.Pro41=
ENST00000488185.2:c.473-1374C=
ENST00000565639.6:n.773+2608C=
ENST00000568591.5:c.2226+2608C=	ENSP00000457162.1:n.2226+2608C=
ENST00000569983.5:n.421+2608C=
NM_000296.3:c.5435C=	NP_000287.3:p.Pro1812=
NM_001009944.2:c.5435C=	NP_001009944.2:p.Pro1812=
XM_005255370.2:c.2390C=	XP_005255427.1:p.Pro797=
XM_011522525.1:c.5513C=	XP_011520827.1:p.Pro1838=
XM_011522526.1:c.5513C=	XP_011520828.1:p.Pro1838=
XM_011522527.1:c.5513C=	XP_011520829.1:p.Pro1838=
XM_011522528.1:c.5489C=	XP_011520830.1:p.Pro1830=
XM_011522529.1:c.5489C=	XP_011520831.1:p.Pro1830=
XM_011522530.1:c.5459C=	XP_011520832.1:p.Pro1820=
XM_011522531.1:c.5441C=	XP_011520833.1:p.Pro1814=
XM_011522532.1:c.5387C=	XP_011520834.1:p.Pro1796=
XM_011522533.1:c.5306C=	XP_011520835.1:p.Pro1769=
XM_011522534.1:c.5249C=	XP_011520836.1:p.Pro1750=
XM_011522535.1:c.3335C=	XP_011520837.1:p.Pro1112=
XM_011522536.1:c.5513C=	XP_011520838.1:p.Pro1838=
XM_011522537.1:c.2513C=	XP_011520839.1:p.Pro838=
XR_932867.1:n.5528C=
XR_932868.1:n.5528C=
XR_932869.1:n.5528C=
XR_932870.1:n.5528C=
XM_005255370.3:c.2390C=	XP_005255427.1:p.Pro797=
XM_011522528.3:c.5489C=	XP_011520830.1:p.Pro1830=
XM_011522529.2:c.5489C=	XP_011520831.1:p.Pro1830=
XM_011522537.2:c.2513C=	XP_011520839.1:p.Pro838=
XM_024450298.1:c.5555C=	XP_024306066.1:p.Pro1852=
XM_024450299.1:c.5483C=	XP_024306067.1:p.Pro1828=
XM_024450300.1:c.5345C=	XP_024306068.1:p.Pro1782=
XM_024450301.1:c.3431C=	XP_024306069.1:p.Pro1144=
NM_000296.4:c.5435C=	NP_000287.4:p.Pro1812=
NM_001009944.3:c.5435C= MANE Select	NP_001009944.3:p.Pro1812=