Canonical Allele Identifier: CA394371195

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2156654T>A (hg19) ; chr16:g.2106653T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106653T>A , CM000678.2:g.2106653T>A	GRCh38
NC_000016.9:g.2156654T>A , CM000678.1:g.2156654T>A	GRCh37
NC_000016.8:g.2096655T>A	NCBI36
NG_008617.1:g.34246A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7234A>T MANE Select	ENSP00000262304.4:p.Asn2412Tyr
ENST00000262304.8:c.7234A>T	ENSP00000262304.4:p.Asn2412Tyr
ENST00000415938.7:n.479A>T
ENST00000423118.5:c.7234A>T	ENSP00000399501.1:p.Asn2412Tyr
ENST00000483024.1:c.402A>T
ENST00000483558.5:n.293A>T
ENST00000483731.5:n.959A>T
ENST00000486339.6:n.980A>T
ENST00000487932.5:c.1921A>T	ENSP00000457132.1:p.Asn641Tyr
ENST00000496574.6:n.1237A>T
ENST00000565639.6:n.942A>T
ENST00000568591.5:c.2395A>T	ENSP00000457162.1:n.2395A>T
ENST00000569983.5:n.590A>T
NM_000296.3:c.7234A>T	NP_000287.3:p.Asn2412Tyr
NM_001009944.2:c.7234A>T	NP_001009944.2:p.Asn2412Tyr
XM_005255370.2:c.4189A>T	XP_005255427.1:p.Asn1397Tyr
XM_011522525.1:c.7312A>T	XP_011520827.1:p.Asn2438Tyr
XM_011522526.1:c.7312A>T	XP_011520828.1:p.Asn2438Tyr
XM_011522527.1:c.7312A>T	XP_011520829.1:p.Asn2438Tyr
XM_011522528.1:c.7288A>T	XP_011520830.1:p.Asn2430Tyr
XM_011522529.1:c.7288A>T	XP_011520831.1:p.Asn2430Tyr
XM_011522530.1:c.7258A>T	XP_011520832.1:p.Asn2420Tyr
XM_011522531.1:c.7240A>T	XP_011520833.1:p.Asn2414Tyr
XM_011522532.1:c.7186A>T	XP_011520834.1:p.Asn2396Tyr
XM_011522533.1:c.7105A>T	XP_011520835.1:p.Asn2369Tyr
XM_011522534.1:c.7048A>T	XP_011520836.1:p.Asn2350Tyr
XM_011522535.1:c.5134A>T	XP_011520837.1:p.Asn1712Tyr
XM_011522536.1:c.7312A>T	XP_011520838.1:p.Asn2438Tyr
XM_011522537.1:c.4312A>T	XP_011520839.1:p.Asn1438Tyr
XR_932867.1:n.7327A>T
XR_932868.1:n.7327A>T
XR_932869.1:n.7327A>T
XR_932870.1:n.7327A>T
XM_005255370.3:c.4189A>T	XP_005255427.1:p.Asn1397Tyr
XM_011522528.3:c.7288A>T	XP_011520830.1:p.Asn2430Tyr
XM_011522529.2:c.7288A>T	XP_011520831.1:p.Asn2430Tyr
XM_011522537.2:c.4312A>T	XP_011520839.1:p.Asn1438Tyr
XM_024450298.1:c.7354A>T	XP_024306066.1:p.Asn2452Tyr
XM_024450299.1:c.7282A>T	XP_024306067.1:p.Asn2428Tyr
XM_024450300.1:c.7144A>T	XP_024306068.1:p.Asn2382Tyr
XM_024450301.1:c.5230A>T	XP_024306069.1:p.Asn1744Tyr
NM_000296.4:c.7234A>T	NP_000287.4:p.Asn2412Tyr
NM_001009944.3:c.7234A>T MANE Select	NP_001009944.3:p.Asn2412Tyr