Canonical Allele Identifier: CA394370173

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2156557T>G (hg19) ; chr16:g.2106556T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106556T>G , CM000678.2:g.2106556T>G	GRCh38
NC_000016.9:g.2156557T>G , CM000678.1:g.2156557T>G	GRCh37
NC_000016.8:g.2096558T>G	NCBI36
NG_008617.1:g.34343A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7331A>C MANE Select	ENSP00000262304.4:p.Tyr2444Ser
ENST00000262304.8:c.7331A>C	ENSP00000262304.4:p.Tyr2444Ser
ENST00000415938.7:n.576A>C
ENST00000423118.5:c.7331A>C	ENSP00000399501.1:p.Tyr2444Ser
ENST00000483558.5:n.390A>C
ENST00000483731.5:n.1056A>C
ENST00000486339.6:n.1077A>C
ENST00000487932.5:c.2018A>C	ENSP00000457132.1:p.Tyr673Ser
ENST00000496574.6:n.1334A>C
ENST00000565639.6:n.1039A>C
ENST00000568591.5:c.2492A>C	ENSP00000457162.1:n.2492A>C
ENST00000569983.5:n.687A>C
NM_000296.3:c.7331A>C	NP_000287.3:p.Tyr2444Ser
NM_001009944.2:c.7331A>C	NP_001009944.2:p.Tyr2444Ser
XM_005255370.2:c.4286A>C	XP_005255427.1:p.Tyr1429Ser
XM_011522525.1:c.7409A>C	XP_011520827.1:p.Tyr2470Ser
XM_011522526.1:c.7409A>C	XP_011520828.1:p.Tyr2470Ser
XM_011522527.1:c.7409A>C	XP_011520829.1:p.Tyr2470Ser
XM_011522528.1:c.7385A>C	XP_011520830.1:p.Tyr2462Ser
XM_011522529.1:c.7385A>C	XP_011520831.1:p.Tyr2462Ser
XM_011522530.1:c.7355A>C	XP_011520832.1:p.Tyr2452Ser
XM_011522531.1:c.7337A>C	XP_011520833.1:p.Tyr2446Ser
XM_011522532.1:c.7283A>C	XP_011520834.1:p.Tyr2428Ser
XM_011522533.1:c.7202A>C	XP_011520835.1:p.Tyr2401Ser
XM_011522534.1:c.7145A>C	XP_011520836.1:p.Tyr2382Ser
XM_011522535.1:c.5231A>C	XP_011520837.1:p.Tyr1744Ser
XM_011522536.1:c.7409A>C	XP_011520838.1:p.Tyr2470Ser
XM_011522537.1:c.4409A>C	XP_011520839.1:p.Tyr1470Ser
XR_932867.1:n.7424A>C
XR_932868.1:n.7424A>C
XR_932869.1:n.7424A>C
XR_932870.1:n.7424A>C
XM_005255370.3:c.4286A>C	XP_005255427.1:p.Tyr1429Ser
XM_011522528.3:c.7385A>C	XP_011520830.1:p.Tyr2462Ser
XM_011522529.2:c.7385A>C	XP_011520831.1:p.Tyr2462Ser
XM_011522537.2:c.4409A>C	XP_011520839.1:p.Tyr1470Ser
XM_024450298.1:c.7451A>C	XP_024306066.1:p.Tyr2484Ser
XM_024450299.1:c.7379A>C	XP_024306067.1:p.Tyr2460Ser
XM_024450300.1:c.7241A>C	XP_024306068.1:p.Tyr2414Ser
XM_024450301.1:c.5327A>C	XP_024306069.1:p.Tyr1776Ser
NM_000296.4:c.7331A>C	NP_000287.4:p.Tyr2444Ser
NM_001009944.3:c.7331A>C MANE Select	NP_001009944.3:p.Tyr2444Ser