Canonical Allele Identifier: CA394370233

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2156566C>A (hg19) ; chr16:g.2106565C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106565C>A , CM000678.2:g.2106565C>A	GRCh38
NC_000016.9:g.2156566C>A , CM000678.1:g.2156566C>A	GRCh37
NC_000016.8:g.2096567C>A	NCBI36
NG_008617.1:g.34334G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7322G>T MANE Select	ENSP00000262304.4:p.Gly2441Val
ENST00000262304.8:c.7322G>T	ENSP00000262304.4:p.Gly2441Val
ENST00000415938.7:n.567G>T
ENST00000423118.5:c.7322G>T	ENSP00000399501.1:p.Gly2441Val
ENST00000483558.5:n.381G>T
ENST00000483731.5:n.1047G>T
ENST00000486339.6:n.1068G>T
ENST00000487932.5:c.2009G>T	ENSP00000457132.1:p.Gly670Val
ENST00000496574.6:n.1325G>T
ENST00000565639.6:n.1030G>T
ENST00000568591.5:c.2483G>T	ENSP00000457162.1:n.2483G>T
ENST00000569983.5:n.678G>T
NM_000296.3:c.7322G>T	NP_000287.3:p.Gly2441Val
NM_001009944.2:c.7322G>T	NP_001009944.2:p.Gly2441Val
XM_005255370.2:c.4277G>T	XP_005255427.1:p.Gly1426Val
XM_011522525.1:c.7400G>T	XP_011520827.1:p.Gly2467Val
XM_011522526.1:c.7400G>T	XP_011520828.1:p.Gly2467Val
XM_011522527.1:c.7400G>T	XP_011520829.1:p.Gly2467Val
XM_011522528.1:c.7376G>T	XP_011520830.1:p.Gly2459Val
XM_011522529.1:c.7376G>T	XP_011520831.1:p.Gly2459Val
XM_011522530.1:c.7346G>T	XP_011520832.1:p.Gly2449Val
XM_011522531.1:c.7328G>T	XP_011520833.1:p.Gly2443Val
XM_011522532.1:c.7274G>T	XP_011520834.1:p.Gly2425Val
XM_011522533.1:c.7193G>T	XP_011520835.1:p.Gly2398Val
XM_011522534.1:c.7136G>T	XP_011520836.1:p.Gly2379Val
XM_011522535.1:c.5222G>T	XP_011520837.1:p.Gly1741Val
XM_011522536.1:c.7400G>T	XP_011520838.1:p.Gly2467Val
XM_011522537.1:c.4400G>T	XP_011520839.1:p.Gly1467Val
XR_932867.1:n.7415G>T
XR_932868.1:n.7415G>T
XR_932869.1:n.7415G>T
XR_932870.1:n.7415G>T
XM_005255370.3:c.4277G>T	XP_005255427.1:p.Gly1426Val
XM_011522528.3:c.7376G>T	XP_011520830.1:p.Gly2459Val
XM_011522529.2:c.7376G>T	XP_011520831.1:p.Gly2459Val
XM_011522537.2:c.4400G>T	XP_011520839.1:p.Gly1467Val
XM_024450298.1:c.7442G>T	XP_024306066.1:p.Gly2481Val
XM_024450299.1:c.7370G>T	XP_024306067.1:p.Gly2457Val
XM_024450300.1:c.7232G>T	XP_024306068.1:p.Gly2411Val
XM_024450301.1:c.5318G>T	XP_024306069.1:p.Gly1773Val
NM_000296.4:c.7322G>T	NP_000287.4:p.Gly2441Val
NM_001009944.3:c.7322G>T MANE Select	NP_001009944.3:p.Gly2441Val