Canonical Allele Identifier: CA2202047742

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111654G= , CM000678.2:g.2111654G=	GRCh38
NC_000016.9:g.2161655G= , CM000678.1:g.2161655G=	GRCh37
NC_000016.8:g.2101656G=	NCBI36
NG_008617.1:g.29245C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3513C= MANE Select	ENSP00000262304.4:p.Thr1171=
ENST00000262304.8:c.3513C=	ENSP00000262304.4:p.Thr1171=
ENST00000415938.7:n.310+686C=
ENST00000423118.5:c.3513C=	ENSP00000399501.1:p.Thr1171=
ENST00000468674.5:n.430+686C=
ENST00000469241.2:n.463C=
ENST00000483024.1:c.233+162C=
ENST00000483731.5:n.790+686C=
ENST00000488185.2:c.473-3296C=
ENST00000565639.6:n.773+686C=
ENST00000568591.5:c.2226+686C=	ENSP00000457162.1:n.2226+686C=
ENST00000569983.5:n.421+686C=
NM_000296.3:c.3513C=	NP_000287.3:p.Thr1171=
NM_001009944.2:c.3513C=	NP_001009944.2:p.Thr1171=
XM_005255370.2:c.468C=	XP_005255427.1:p.Thr156=
XM_011522525.1:c.3591C=	XP_011520827.1:p.Thr1197=
XM_011522526.1:c.3591C=	XP_011520828.1:p.Thr1197=
XM_011522527.1:c.3591C=	XP_011520829.1:p.Thr1197=
XM_011522528.1:c.3567C=	XP_011520830.1:p.Thr1189=
XM_011522529.1:c.3567C=	XP_011520831.1:p.Thr1189=
XM_011522530.1:c.3537C=	XP_011520832.1:p.Thr1179=
XM_011522531.1:c.3519C=	XP_011520833.1:p.Thr1173=
XM_011522532.1:c.3465C=	XP_011520834.1:p.Thr1155=
XM_011522533.1:c.3384C=	XP_011520835.1:p.Thr1128=
XM_011522534.1:c.3327C=	XP_011520836.1:p.Thr1109=
XM_011522535.1:c.1413C=	XP_011520837.1:p.Thr471=
XM_011522536.1:c.3591C=	XP_011520838.1:p.Thr1197=
XM_011522537.1:c.591C=	XP_011520839.1:p.Thr197=
XR_932867.1:n.3606C=
XR_932868.1:n.3606C=
XR_932869.1:n.3606C=
XR_932870.1:n.3606C=
XM_005255370.3:c.468C=	XP_005255427.1:p.Thr156=
XM_011522528.3:c.3567C=	XP_011520830.1:p.Thr1189=
XM_011522529.2:c.3567C=	XP_011520831.1:p.Thr1189=
XM_011522537.2:c.591C=	XP_011520839.1:p.Thr197=
XM_024450298.1:c.3633C=	XP_024306066.1:p.Thr1211=
XM_024450299.1:c.3561C=	XP_024306067.1:p.Thr1187=
XM_024450300.1:c.3423C=	XP_024306068.1:p.Thr1141=
XM_024450301.1:c.1509C=	XP_024306069.1:p.Thr503=
NM_000296.4:c.3513C=	NP_000287.4:p.Thr1171=
NM_001009944.3:c.3513C= MANE Select	NP_001009944.3:p.Thr1171=