Canonical Allele Identifier: CA394382739

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2161545A>T (hg19) ; chr16:g.2111544A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111544A>T , CM000678.2:g.2111544A>T	GRCh38
NC_000016.9:g.2161545A>T , CM000678.1:g.2161545A>T	GRCh37
NC_000016.8:g.2101546A>T	NCBI36
NG_008617.1:g.29355T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3623T>A MANE Select	ENSP00000262304.4:p.Val1208Asp
ENST00000262304.8:c.3623T>A	ENSP00000262304.4:p.Val1208Asp
ENST00000415938.7:n.310+796T>A
ENST00000423118.5:c.3623T>A	ENSP00000399501.1:p.Val1208Asp
ENST00000468674.5:n.430+796T>A
ENST00000469241.2:n.573T>A
ENST00000483024.1:c.233+272T>A
ENST00000483731.5:n.790+796T>A
ENST00000488185.2:c.473-3186T>A
ENST00000565639.6:n.773+796T>A
ENST00000568591.5:c.2226+796T>A	ENSP00000457162.1:n.2226+796T>A
ENST00000569983.5:n.421+796T>A
NM_000296.3:c.3623T>A	NP_000287.3:p.Val1208Asp
NM_001009944.2:c.3623T>A	NP_001009944.2:p.Val1208Asp
XM_005255370.2:c.578T>A	XP_005255427.1:p.Val193Asp
XM_011522525.1:c.3701T>A	XP_011520827.1:p.Val1234Asp
XM_011522526.1:c.3701T>A	XP_011520828.1:p.Val1234Asp
XM_011522527.1:c.3701T>A	XP_011520829.1:p.Val1234Asp
XM_011522528.1:c.3677T>A	XP_011520830.1:p.Val1226Asp
XM_011522529.1:c.3677T>A	XP_011520831.1:p.Val1226Asp
XM_011522530.1:c.3647T>A	XP_011520832.1:p.Val1216Asp
XM_011522531.1:c.3629T>A	XP_011520833.1:p.Val1210Asp
XM_011522532.1:c.3575T>A	XP_011520834.1:p.Val1192Asp
XM_011522533.1:c.3494T>A	XP_011520835.1:p.Val1165Asp
XM_011522534.1:c.3437T>A	XP_011520836.1:p.Val1146Asp
XM_011522535.1:c.1523T>A	XP_011520837.1:p.Val508Asp
XM_011522536.1:c.3701T>A	XP_011520838.1:p.Val1234Asp
XM_011522537.1:c.701T>A	XP_011520839.1:p.Val234Asp
XR_932867.1:n.3716T>A
XR_932868.1:n.3716T>A
XR_932869.1:n.3716T>A
XR_932870.1:n.3716T>A
XM_005255370.3:c.578T>A	XP_005255427.1:p.Val193Asp
XM_011522528.3:c.3677T>A	XP_011520830.1:p.Val1226Asp
XM_011522529.2:c.3677T>A	XP_011520831.1:p.Val1226Asp
XM_011522537.2:c.701T>A	XP_011520839.1:p.Val234Asp
XM_024450298.1:c.3743T>A	XP_024306066.1:p.Val1248Asp
XM_024450299.1:c.3671T>A	XP_024306067.1:p.Val1224Asp
XM_024450300.1:c.3533T>A	XP_024306068.1:p.Val1178Asp
XM_024450301.1:c.1619T>A	XP_024306069.1:p.Val540Asp
NM_000296.4:c.3623T>A	NP_000287.4:p.Val1208Asp
NM_001009944.3:c.3623T>A MANE Select	NP_001009944.3:p.Val1208Asp