Canonical Allele Identifier: CA493046772

Gene: PKD1

Linked Data

• gnomAD v4: 16-2106584-G-T
• MyVariant Identifiers: chr16:g.2156585G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106584G>T , CM000678.2:g.2106584G>T	GRCh38
NC_000016.9:g.2156585G>T , CM000678.1:g.2156585G>T	GRCh37
NC_000016.8:g.2096586G>T	NCBI36
NG_008617.1:g.34315C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7303C>A MANE Select	ENSP00000262304.4:p.Arg2435=
ENST00000262304.8:c.7303C>A	ENSP00000262304.4:p.Arg2435=
ENST00000415938.7:n.548C>A
ENST00000423118.5:c.7303C>A	ENSP00000399501.1:p.Arg2435=
ENST00000483558.5:n.362C>A
ENST00000483731.5:n.1028C>A
ENST00000486339.6:n.1049C>A
ENST00000487932.5:c.1990C>A	ENSP00000457132.1:p.Arg664=
ENST00000496574.6:n.1306C>A
ENST00000565639.6:n.1011C>A
ENST00000568591.5:c.2464C>A	ENSP00000457162.1:n.2464C>A
ENST00000569983.5:n.659C>A
NM_000296.3:c.7303C>A	NP_000287.3:p.Arg2435=
NM_001009944.2:c.7303C>A	NP_001009944.2:p.Arg2435=
XM_005255370.2:c.4258C>A	XP_005255427.1:p.Arg1420=
XM_011522525.1:c.7381C>A	XP_011520827.1:p.Arg2461=
XM_011522526.1:c.7381C>A	XP_011520828.1:p.Arg2461=
XM_011522527.1:c.7381C>A	XP_011520829.1:p.Arg2461=
XM_011522528.1:c.7357C>A	XP_011520830.1:p.Arg2453=
XM_011522529.1:c.7357C>A	XP_011520831.1:p.Arg2453=
XM_011522530.1:c.7327C>A	XP_011520832.1:p.Arg2443=
XM_011522531.1:c.7309C>A	XP_011520833.1:p.Arg2437=
XM_011522532.1:c.7255C>A	XP_011520834.1:p.Arg2419=
XM_011522533.1:c.7174C>A	XP_011520835.1:p.Arg2392=
XM_011522534.1:c.7117C>A	XP_011520836.1:p.Arg2373=
XM_011522535.1:c.5203C>A	XP_011520837.1:p.Arg1735=
XM_011522536.1:c.7381C>A	XP_011520838.1:p.Arg2461=
XM_011522537.1:c.4381C>A	XP_011520839.1:p.Arg1461=
XR_932867.1:n.7396C>A
XR_932868.1:n.7396C>A
XR_932869.1:n.7396C>A
XR_932870.1:n.7396C>A
XM_005255370.3:c.4258C>A	XP_005255427.1:p.Arg1420=
XM_011522528.3:c.7357C>A	XP_011520830.1:p.Arg2453=
XM_011522529.2:c.7357C>A	XP_011520831.1:p.Arg2453=
XM_011522537.2:c.4381C>A	XP_011520839.1:p.Arg1461=
XM_024450298.1:c.7423C>A	XP_024306066.1:p.Arg2475=
XM_024450299.1:c.7351C>A	XP_024306067.1:p.Arg2451=
XM_024450300.1:c.7213C>A	XP_024306068.1:p.Arg2405=
XM_024450301.1:c.5299C>A	XP_024306069.1:p.Arg1767=
NM_000296.4:c.7303C>A	NP_000287.4:p.Arg2435=
NM_001009944.3:c.7303C>A MANE Select	NP_001009944.3:p.Arg2435=