Canonical Allele Identifier: CA394393062

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2167833G>C (hg19) ; chr16:g.2117832G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2117832G>C , CM000678.2:g.2117832G>C	GRCh38
NC_000016.9:g.2167833G>C , CM000678.1:g.2167833G>C	GRCh37
NC_000016.8:g.2107834G>C	NCBI36
NG_008617.1:g.23067C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262304.9:c.1160C>G MANE Select	ENSP00000262304.4:p.Ala387Gly
ENST00000262304.8:c.1160C>G	ENSP00000262304.4:p.Ala387Gly
ENST00000423118.5:c.1160C>G	ENSP00000399501.1:p.Ala387Gly
ENST00000488185.2:c.247C>G
ENST00000568591.5:c.128C>G	ENSP00000457162.1:p.Ala43Gly
ENST00000570150.1:n.293C>G
NM_000296.3:c.1160C>G	NP_000287.3:p.Ala387Gly
NM_001009944.2:c.1160C>G	NP_001009944.2:p.Ala387Gly
XM_011522525.1:c.1214C>G	XP_011520827.1:p.Ala405Gly
XM_011522526.1:c.1214C>G	XP_011520828.1:p.Ala405Gly
XM_011522527.1:c.1214C>G	XP_011520829.1:p.Ala405Gly
XM_011522528.1:c.1214C>G	XP_011520830.1:p.Ala405Gly
XM_011522529.1:c.1214C>G	XP_011520831.1:p.Ala405Gly
XM_011522530.1:c.1160C>G	XP_011520832.1:p.Ala387Gly
XM_011522531.1:c.1142C>G	XP_011520833.1:p.Ala381Gly
XM_011522532.1:c.1088C>G	XP_011520834.1:p.Ala363Gly
XM_011522533.1:c.1007C>G	XP_011520835.1:p.Ala336Gly
XM_011522534.1:c.950C>G	XP_011520836.1:p.Ala317Gly
XM_011522536.1:c.1214C>G	XP_011520838.1:p.Ala405Gly
XR_932867.1:n.1229C>G
XR_932868.1:n.1229C>G
XR_932869.1:n.1229C>G
XR_932870.1:n.1229C>G
XM_011522528.3:c.1214C>G	XP_011520830.1:p.Ala405Gly
XM_011522529.2:c.1214C>G	XP_011520831.1:p.Ala405Gly
XM_024450298.1:c.1160C>G	XP_024306066.1:p.Ala387Gly
XM_024450299.1:c.1088C>G	XP_024306067.1:p.Ala363Gly
XM_024450300.1:c.950C>G	XP_024306068.1:p.Ala317Gly
NM_000296.4:c.1160C>G	NP_000287.4:p.Ala387Gly
NM_001009944.3:c.1160C>G MANE Select	NP_001009944.3:p.Ala387Gly