Canonical Allele Identifier: CA493046753
Gene: PKD1 HGNC NCBI

Linked Data

dbSNP Id: rs764386011
MyVariant Identifiers: chr16:g.2156565G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106564G>C , CM000678.2:g.2106564G>C GRCh38
NC_000016.9:g.2156565G>C , CM000678.1:g.2156565G>C GRCh37
NC_000016.8:g.2096566G>C NCBI36
NG_008617.1:g.34335C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7323C>G MANE Select ENSP00000262304.4:p.Gly2441=
ENST00000262304.8:c.7323C>G ENSP00000262304.4:p.Gly2441=
ENST00000415938.7:n.568C>G
ENST00000423118.5:c.7323C>G ENSP00000399501.1:p.Gly2441=
ENST00000483558.5:n.382C>G
ENST00000483731.5:n.1048C>G
ENST00000486339.6:n.1069C>G
ENST00000487932.5:c.2010C>G ENSP00000457132.1:p.Gly670=
ENST00000496574.6:n.1326C>G
ENST00000565639.6:n.1031C>G
ENST00000568591.5:c.2484C>G ENSP00000457162.1:n.2484C>G
ENST00000569983.5:n.679C>G
NM_000296.3:c.7323C>G NP_000287.3:p.Gly2441=
NM_001009944.2:c.7323C>G NP_001009944.2:p.Gly2441=
XM_005255370.2:c.4278C>G XP_005255427.1:p.Gly1426=
XM_011522525.1:c.7401C>G XP_011520827.1:p.Gly2467=
XM_011522526.1:c.7401C>G XP_011520828.1:p.Gly2467=
XM_011522527.1:c.7401C>G XP_011520829.1:p.Gly2467=
XM_011522528.1:c.7377C>G XP_011520830.1:p.Gly2459=
XM_011522529.1:c.7377C>G XP_011520831.1:p.Gly2459=
XM_011522530.1:c.7347C>G XP_011520832.1:p.Gly2449=
XM_011522531.1:c.7329C>G XP_011520833.1:p.Gly2443=
XM_011522532.1:c.7275C>G XP_011520834.1:p.Gly2425=
XM_011522533.1:c.7194C>G XP_011520835.1:p.Gly2398=
XM_011522534.1:c.7137C>G XP_011520836.1:p.Gly2379=
XM_011522535.1:c.5223C>G XP_011520837.1:p.Gly1741=
XM_011522536.1:c.7401C>G XP_011520838.1:p.Gly2467=
XM_011522537.1:c.4401C>G XP_011520839.1:p.Gly1467=
XR_932867.1:n.7416C>G
XR_932868.1:n.7416C>G
XR_932869.1:n.7416C>G
XR_932870.1:n.7416C>G
XM_005255370.3:c.4278C>G XP_005255427.1:p.Gly1426=
XM_011522528.3:c.7377C>G XP_011520830.1:p.Gly2459=
XM_011522529.2:c.7377C>G XP_011520831.1:p.Gly2459=
XM_011522537.2:c.4401C>G XP_011520839.1:p.Gly1467=
XM_024450298.1:c.7443C>G XP_024306066.1:p.Gly2481=
XM_024450299.1:c.7371C>G XP_024306067.1:p.Gly2457=
XM_024450300.1:c.7233C>G XP_024306068.1:p.Gly2411=
XM_024450301.1:c.5319C>G XP_024306069.1:p.Gly1773=
NM_000296.4:c.7323C>G NP_000287.4:p.Gly2441=
NM_001009944.3:c.7323C>G MANE Select NP_001009944.3:p.Gly2441=