Canonical Allele Identifier: CA2202035363

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106615C= , CM000678.2:g.2106615C=	GRCh38
NC_000016.9:g.2156616C= , CM000678.1:g.2156616C=	GRCh37
NC_000016.8:g.2096617C=	NCBI36
NG_008617.1:g.34284G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7272G= MANE Select	ENSP00000262304.4:p.Thr2424=
ENST00000262304.8:c.7272G=	ENSP00000262304.4:p.Thr2424=
ENST00000415938.7:n.517G=
ENST00000423118.5:c.7272G=	ENSP00000399501.1:p.Thr2424=
ENST00000483024.1:c.440G=
ENST00000483558.5:n.331G=
ENST00000483731.5:n.997G=
ENST00000486339.6:n.1018G=
ENST00000487932.5:c.1959G=	ENSP00000457132.1:p.Thr653=
ENST00000496574.6:n.1275G=
ENST00000565639.6:n.980G=
ENST00000568591.5:c.2433G=	ENSP00000457162.1:n.2433G=
ENST00000569983.5:n.628G=
NM_000296.3:c.7272G=	NP_000287.3:p.Thr2424=
NM_001009944.2:c.7272G=	NP_001009944.2:p.Thr2424=
XM_005255370.2:c.4227G=	XP_005255427.1:p.Thr1409=
XM_011522525.1:c.7350G=	XP_011520827.1:p.Thr2450=
XM_011522526.1:c.7350G=	XP_011520828.1:p.Thr2450=
XM_011522527.1:c.7350G=	XP_011520829.1:p.Thr2450=
XM_011522528.1:c.7326G=	XP_011520830.1:p.Thr2442=
XM_011522529.1:c.7326G=	XP_011520831.1:p.Thr2442=
XM_011522530.1:c.7296G=	XP_011520832.1:p.Thr2432=
XM_011522531.1:c.7278G=	XP_011520833.1:p.Thr2426=
XM_011522532.1:c.7224G=	XP_011520834.1:p.Thr2408=
XM_011522533.1:c.7143G=	XP_011520835.1:p.Thr2381=
XM_011522534.1:c.7086G=	XP_011520836.1:p.Thr2362=
XM_011522535.1:c.5172G=	XP_011520837.1:p.Thr1724=
XM_011522536.1:c.7350G=	XP_011520838.1:p.Thr2450=
XM_011522537.1:c.4350G=	XP_011520839.1:p.Thr1450=
XR_932867.1:n.7365G=
XR_932868.1:n.7365G=
XR_932869.1:n.7365G=
XR_932870.1:n.7365G=
XM_005255370.3:c.4227G=	XP_005255427.1:p.Thr1409=
XM_011522528.3:c.7326G=	XP_011520830.1:p.Thr2442=
XM_011522529.2:c.7326G=	XP_011520831.1:p.Thr2442=
XM_011522537.2:c.4350G=	XP_011520839.1:p.Thr1450=
XM_024450298.1:c.7392G=	XP_024306066.1:p.Thr2464=
XM_024450299.1:c.7320G=	XP_024306067.1:p.Thr2440=
XM_024450300.1:c.7182G=	XP_024306068.1:p.Thr2394=
XM_024450301.1:c.5268G=	XP_024306069.1:p.Thr1756=
NM_000296.4:c.7272G=	NP_000287.4:p.Thr2424=
NM_001009944.3:c.7272G= MANE Select	NP_001009944.3:p.Thr2424=