Canonical Allele Identifier: CA394370250

Gene: PKD1

Linked Data

• gnomAD v4: 16-2106568-T-A
• MyVariant Identifiers: chr16:g.2156569T>A (hg19) ; chr16:g.2106568T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106568T>A , CM000678.2:g.2106568T>A	GRCh38
NC_000016.9:g.2156569T>A , CM000678.1:g.2156569T>A	GRCh37
NC_000016.8:g.2096570T>A	NCBI36
NG_008617.1:g.34331A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7319A>T MANE Select	ENSP00000262304.4:p.Asp2440Val
ENST00000262304.8:c.7319A>T	ENSP00000262304.4:p.Asp2440Val
ENST00000415938.7:n.564A>T
ENST00000423118.5:c.7319A>T	ENSP00000399501.1:p.Asp2440Val
ENST00000483558.5:n.378A>T
ENST00000483731.5:n.1044A>T
ENST00000486339.6:n.1065A>T
ENST00000487932.5:c.2006A>T	ENSP00000457132.1:p.Asp669Val
ENST00000496574.6:n.1322A>T
ENST00000565639.6:n.1027A>T
ENST00000568591.5:c.2480A>T	ENSP00000457162.1:n.2480A>T
ENST00000569983.5:n.675A>T
NM_000296.3:c.7319A>T	NP_000287.3:p.Asp2440Val
NM_001009944.2:c.7319A>T	NP_001009944.2:p.Asp2440Val
XM_005255370.2:c.4274A>T	XP_005255427.1:p.Asp1425Val
XM_011522525.1:c.7397A>T	XP_011520827.1:p.Asp2466Val
XM_011522526.1:c.7397A>T	XP_011520828.1:p.Asp2466Val
XM_011522527.1:c.7397A>T	XP_011520829.1:p.Asp2466Val
XM_011522528.1:c.7373A>T	XP_011520830.1:p.Asp2458Val
XM_011522529.1:c.7373A>T	XP_011520831.1:p.Asp2458Val
XM_011522530.1:c.7343A>T	XP_011520832.1:p.Asp2448Val
XM_011522531.1:c.7325A>T	XP_011520833.1:p.Asp2442Val
XM_011522532.1:c.7271A>T	XP_011520834.1:p.Asp2424Val
XM_011522533.1:c.7190A>T	XP_011520835.1:p.Asp2397Val
XM_011522534.1:c.7133A>T	XP_011520836.1:p.Asp2378Val
XM_011522535.1:c.5219A>T	XP_011520837.1:p.Asp1740Val
XM_011522536.1:c.7397A>T	XP_011520838.1:p.Asp2466Val
XM_011522537.1:c.4397A>T	XP_011520839.1:p.Asp1466Val
XR_932867.1:n.7412A>T
XR_932868.1:n.7412A>T
XR_932869.1:n.7412A>T
XR_932870.1:n.7412A>T
XM_005255370.3:c.4274A>T	XP_005255427.1:p.Asp1425Val
XM_011522528.3:c.7373A>T	XP_011520830.1:p.Asp2458Val
XM_011522529.2:c.7373A>T	XP_011520831.1:p.Asp2458Val
XM_011522537.2:c.4397A>T	XP_011520839.1:p.Asp1466Val
XM_024450298.1:c.7439A>T	XP_024306066.1:p.Asp2480Val
XM_024450299.1:c.7367A>T	XP_024306067.1:p.Asp2456Val
XM_024450300.1:c.7229A>T	XP_024306068.1:p.Asp2410Val
XM_024450301.1:c.5315A>T	XP_024306069.1:p.Asp1772Val
NM_000296.4:c.7319A>T	NP_000287.4:p.Asp2440Val
NM_001009944.3:c.7319A>T MANE Select	NP_001009944.3:p.Asp2440Val