Canonical Allele Identifier: CA2202049797

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114574C= , CM000678.2:g.2114574C=	GRCh38
NC_000016.9:g.2164575C= , CM000678.1:g.2164575C=	GRCh37
NC_000016.8:g.2104576C=	NCBI36
NG_008617.1:g.26325G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2449G= MANE Select	ENSP00000262304.4:p.Val817=
ENST00000262304.8:c.2449G=	ENSP00000262304.4:p.Val817=
ENST00000423118.5:c.2449G=	ENSP00000399501.1:p.Val817=
ENST00000488185.2:c.472+2915G=
ENST00000568591.5:c.1380G=	ENSP00000457162.1:n.1380G=
NM_000296.3:c.2449G=	NP_000287.3:p.Val817=
NM_001009944.2:c.2449G=	NP_001009944.2:p.Val817=
XM_011522525.1:c.2503G=	XP_011520827.1:p.Val835=
XM_011522526.1:c.2503G=	XP_011520828.1:p.Val835=
XM_011522527.1:c.2503G=	XP_011520829.1:p.Val835=
XM_011522528.1:c.2503G=	XP_011520830.1:p.Val835=
XM_011522529.1:c.2503G=	XP_011520831.1:p.Val835=
XM_011522530.1:c.2449G=	XP_011520832.1:p.Val817=
XM_011522531.1:c.2431G=	XP_011520833.1:p.Val811=
XM_011522532.1:c.2377G=	XP_011520834.1:p.Val793=
XM_011522533.1:c.2296G=	XP_011520835.1:p.Val766=
XM_011522534.1:c.2239G=	XP_011520836.1:p.Val747=
XM_011522535.1:c.325G=	XP_011520837.1:p.Val109=
XM_011522536.1:c.2503G=	XP_011520838.1:p.Val835=
XR_932867.1:n.2518G=
XR_932868.1:n.2518G=
XR_932869.1:n.2518G=
XR_932870.1:n.2518G=
XM_005255370.3:c.-601G=	XP_005255427.1:n.-601G=
XM_011522528.3:c.2503G=	XP_011520830.1:p.Val835=
XM_011522529.2:c.2503G=	XP_011520831.1:p.Val835=
XM_024450298.1:c.2449G=	XP_024306066.1:p.Val817=
XM_024450299.1:c.2377G=	XP_024306067.1:p.Val793=
XM_024450300.1:c.2239G=	XP_024306068.1:p.Val747=
XM_024450301.1:c.325G=	XP_024306069.1:p.Val109=
NM_000296.4:c.2449G=	NP_000287.4:p.Val817=
NM_001009944.3:c.2449G= MANE Select	NP_001009944.3:p.Val817=