Canonical Allele Identifier: CA2202051929

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2117830C= , CM000678.2:g.2117830C=	GRCh38
NC_000016.9:g.2167831C= , CM000678.1:g.2167831C=	GRCh37
NC_000016.8:g.2107832C=	NCBI36
NG_008617.1:g.23069G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262304.9:c.1162G= MANE Select	ENSP00000262304.4:p.Ala388=
ENST00000262304.8:c.1162G=	ENSP00000262304.4:p.Ala388=
ENST00000423118.5:c.1162G=	ENSP00000399501.1:p.Ala388=
ENST00000488185.2:c.249G=
ENST00000568591.5:c.130G=	ENSP00000457162.1:p.Ala44=
ENST00000570150.1:n.295G=
NM_000296.3:c.1162G=	NP_000287.3:p.Ala388=
NM_001009944.2:c.1162G=	NP_001009944.2:p.Ala388=
XM_011522525.1:c.1216G=	XP_011520827.1:p.Ala406=
XM_011522526.1:c.1216G=	XP_011520828.1:p.Ala406=
XM_011522527.1:c.1216G=	XP_011520829.1:p.Ala406=
XM_011522528.1:c.1216G=	XP_011520830.1:p.Ala406=
XM_011522529.1:c.1216G=	XP_011520831.1:p.Ala406=
XM_011522530.1:c.1162G=	XP_011520832.1:p.Ala388=
XM_011522531.1:c.1144G=	XP_011520833.1:p.Ala382=
XM_011522532.1:c.1090G=	XP_011520834.1:p.Ala364=
XM_011522533.1:c.1009G=	XP_011520835.1:p.Ala337=
XM_011522534.1:c.952G=	XP_011520836.1:p.Ala318=
XM_011522536.1:c.1216G=	XP_011520838.1:p.Ala406=
XR_932867.1:n.1231G=
XR_932868.1:n.1231G=
XR_932869.1:n.1231G=
XR_932870.1:n.1231G=
XM_011522528.3:c.1216G=	XP_011520830.1:p.Ala406=
XM_011522529.2:c.1216G=	XP_011520831.1:p.Ala406=
XM_024450298.1:c.1162G=	XP_024306066.1:p.Ala388=
XM_024450299.1:c.1090G=	XP_024306067.1:p.Ala364=
XM_024450300.1:c.952G=	XP_024306068.1:p.Ala318=
NM_000296.4:c.1162G=	NP_000287.4:p.Ala388=
NM_001009944.3:c.1162G= MANE Select	NP_001009944.3:p.Ala388=