Canonical Allele Identifier: CA492976304

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2166835T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2116834T>G , CM000678.2:g.2116834T>G	GRCh38
NC_000016.9:g.2166835T>G , CM000678.1:g.2166835T>G	GRCh37
NC_000016.8:g.2106836T>G	NCBI36
NG_008617.1:g.24065A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262304.9:c.1605A>C MANE Select	ENSP00000262304.4:p.Gly535=
ENST00000262304.8:c.1605A>C	ENSP00000262304.4:p.Gly535=
ENST00000423118.5:c.1605A>C	ENSP00000399501.1:p.Gly535=
ENST00000488185.2:c.472+655A>C
ENST00000568591.5:c.536A>C	ENSP00000457162.1:p.Glu179Ala
ENST00000570150.1:n.519-190A>C
NM_000296.3:c.1605A>C	NP_000287.3:p.Gly535=
NM_001009944.2:c.1605A>C	NP_001009944.2:p.Gly535=
XM_011522525.1:c.1659A>C	XP_011520827.1:p.Gly553=
XM_011522526.1:c.1659A>C	XP_011520828.1:p.Gly553=
XM_011522527.1:c.1659A>C	XP_011520829.1:p.Gly553=
XM_011522528.1:c.1659A>C	XP_011520830.1:p.Gly553=
XM_011522529.1:c.1659A>C	XP_011520831.1:p.Gly553=
XM_011522530.1:c.1605A>C	XP_011520832.1:p.Gly535=
XM_011522531.1:c.1587A>C	XP_011520833.1:p.Gly529=
XM_011522532.1:c.1533A>C	XP_011520834.1:p.Gly511=
XM_011522533.1:c.1452A>C	XP_011520835.1:p.Gly484=
XM_011522534.1:c.1395A>C	XP_011520836.1:p.Gly465=
XM_011522536.1:c.1659A>C	XP_011520838.1:p.Gly553=
XR_932867.1:n.1674A>C
XR_932868.1:n.1674A>C
XR_932869.1:n.1674A>C
XR_932870.1:n.1674A>C
XM_011522528.3:c.1659A>C	XP_011520830.1:p.Gly553=
XM_011522529.2:c.1659A>C	XP_011520831.1:p.Gly553=
XM_024450298.1:c.1605A>C	XP_024306066.1:p.Gly535=
XM_024450299.1:c.1533A>C	XP_024306067.1:p.Gly511=
XM_024450300.1:c.1395A>C	XP_024306068.1:p.Gly465=
NM_000296.4:c.1605A>C	NP_000287.4:p.Gly535=
NM_001009944.3:c.1605A>C MANE Select	NP_001009944.3:p.Gly535=