Canonical Allele Identifier: CA394371247

Gene: PKD1

Linked Data

• gnomAD v4: 16-2106664-C-A
• MyVariant Identifiers: chr16:g.2156665C>A (hg19) ; chr16:g.2106664C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106664C>A , CM000678.2:g.2106664C>A	GRCh38
NC_000016.9:g.2156665C>A , CM000678.1:g.2156665C>A	GRCh37
NC_000016.8:g.2096666C>A	NCBI36
NG_008617.1:g.34235G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7223G>T MANE Select	ENSP00000262304.4:p.Arg2408Leu
ENST00000262304.8:c.7223G>T	ENSP00000262304.4:p.Arg2408Leu
ENST00000415938.7:n.468G>T
ENST00000423118.5:c.7223G>T	ENSP00000399501.1:p.Arg2408Leu
ENST00000483024.1:c.391G>T
ENST00000483558.5:n.282G>T
ENST00000483731.5:n.948G>T
ENST00000486339.6:n.969G>T
ENST00000487932.5:c.1910G>T	ENSP00000457132.1:p.Arg637Leu
ENST00000496574.6:n.1226G>T
ENST00000565639.6:n.931G>T
ENST00000568591.5:c.2384G>T	ENSP00000457162.1:n.2384G>T
ENST00000569983.5:n.579G>T
NM_000296.3:c.7223G>T	NP_000287.3:p.Arg2408Leu
NM_001009944.2:c.7223G>T	NP_001009944.2:p.Arg2408Leu
XM_005255370.2:c.4178G>T	XP_005255427.1:p.Arg1393Leu
XM_011522525.1:c.7301G>T	XP_011520827.1:p.Arg2434Leu
XM_011522526.1:c.7301G>T	XP_011520828.1:p.Arg2434Leu
XM_011522527.1:c.7301G>T	XP_011520829.1:p.Arg2434Leu
XM_011522528.1:c.7277G>T	XP_011520830.1:p.Arg2426Leu
XM_011522529.1:c.7277G>T	XP_011520831.1:p.Arg2426Leu
XM_011522530.1:c.7247G>T	XP_011520832.1:p.Arg2416Leu
XM_011522531.1:c.7229G>T	XP_011520833.1:p.Arg2410Leu
XM_011522532.1:c.7175G>T	XP_011520834.1:p.Arg2392Leu
XM_011522533.1:c.7094G>T	XP_011520835.1:p.Arg2365Leu
XM_011522534.1:c.7037G>T	XP_011520836.1:p.Arg2346Leu
XM_011522535.1:c.5123G>T	XP_011520837.1:p.Arg1708Leu
XM_011522536.1:c.7301G>T	XP_011520838.1:p.Arg2434Leu
XM_011522537.1:c.4301G>T	XP_011520839.1:p.Arg1434Leu
XR_932867.1:n.7316G>T
XR_932868.1:n.7316G>T
XR_932869.1:n.7316G>T
XR_932870.1:n.7316G>T
XM_005255370.3:c.4178G>T	XP_005255427.1:p.Arg1393Leu
XM_011522528.3:c.7277G>T	XP_011520830.1:p.Arg2426Leu
XM_011522529.2:c.7277G>T	XP_011520831.1:p.Arg2426Leu
XM_011522537.2:c.4301G>T	XP_011520839.1:p.Arg1434Leu
XM_024450298.1:c.7343G>T	XP_024306066.1:p.Arg2448Leu
XM_024450299.1:c.7271G>T	XP_024306067.1:p.Arg2424Leu
XM_024450300.1:c.7133G>T	XP_024306068.1:p.Arg2378Leu
XM_024450301.1:c.5219G>T	XP_024306069.1:p.Arg1740Leu
NM_000296.4:c.7223G>T	NP_000287.4:p.Arg2408Leu
NM_001009944.3:c.7223G>T MANE Select	NP_001009944.3:p.Arg2408Leu