Canonical Allele Identifier: CA394371244

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2156663T>C (hg19) ; chr16:g.2106662T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106662T>C , CM000678.2:g.2106662T>C	GRCh38
NC_000016.9:g.2156663T>C , CM000678.1:g.2156663T>C	GRCh37
NC_000016.8:g.2096664T>C	NCBI36
NG_008617.1:g.34237A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7225A>G MANE Select	ENSP00000262304.4:p.Thr2409Ala
ENST00000262304.8:c.7225A>G	ENSP00000262304.4:p.Thr2409Ala
ENST00000415938.7:n.470A>G
ENST00000423118.5:c.7225A>G	ENSP00000399501.1:p.Thr2409Ala
ENST00000483024.1:c.393A>G
ENST00000483558.5:n.284A>G
ENST00000483731.5:n.950A>G
ENST00000486339.6:n.971A>G
ENST00000487932.5:c.1912A>G	ENSP00000457132.1:p.Thr638Ala
ENST00000496574.6:n.1228A>G
ENST00000565639.6:n.933A>G
ENST00000568591.5:c.2386A>G	ENSP00000457162.1:n.2386A>G
ENST00000569983.5:n.581A>G
NM_000296.3:c.7225A>G	NP_000287.3:p.Thr2409Ala
NM_001009944.2:c.7225A>G	NP_001009944.2:p.Thr2409Ala
XM_005255370.2:c.4180A>G	XP_005255427.1:p.Thr1394Ala
XM_011522525.1:c.7303A>G	XP_011520827.1:p.Thr2435Ala
XM_011522526.1:c.7303A>G	XP_011520828.1:p.Thr2435Ala
XM_011522527.1:c.7303A>G	XP_011520829.1:p.Thr2435Ala
XM_011522528.1:c.7279A>G	XP_011520830.1:p.Thr2427Ala
XM_011522529.1:c.7279A>G	XP_011520831.1:p.Thr2427Ala
XM_011522530.1:c.7249A>G	XP_011520832.1:p.Thr2417Ala
XM_011522531.1:c.7231A>G	XP_011520833.1:p.Thr2411Ala
XM_011522532.1:c.7177A>G	XP_011520834.1:p.Thr2393Ala
XM_011522533.1:c.7096A>G	XP_011520835.1:p.Thr2366Ala
XM_011522534.1:c.7039A>G	XP_011520836.1:p.Thr2347Ala
XM_011522535.1:c.5125A>G	XP_011520837.1:p.Thr1709Ala
XM_011522536.1:c.7303A>G	XP_011520838.1:p.Thr2435Ala
XM_011522537.1:c.4303A>G	XP_011520839.1:p.Thr1435Ala
XR_932867.1:n.7318A>G
XR_932868.1:n.7318A>G
XR_932869.1:n.7318A>G
XR_932870.1:n.7318A>G
XM_005255370.3:c.4180A>G	XP_005255427.1:p.Thr1394Ala
XM_011522528.3:c.7279A>G	XP_011520830.1:p.Thr2427Ala
XM_011522529.2:c.7279A>G	XP_011520831.1:p.Thr2427Ala
XM_011522537.2:c.4303A>G	XP_011520839.1:p.Thr1435Ala
XM_024450298.1:c.7345A>G	XP_024306066.1:p.Thr2449Ala
XM_024450299.1:c.7273A>G	XP_024306067.1:p.Thr2425Ala
XM_024450300.1:c.7135A>G	XP_024306068.1:p.Thr2379Ala
XM_024450301.1:c.5221A>G	XP_024306069.1:p.Thr1741Ala
NM_000296.4:c.7225A>G	NP_000287.4:p.Thr2409Ala
NM_001009944.3:c.7225A>G MANE Select	NP_001009944.3:p.Thr2409Ala