Canonical Allele Identifier: CA394387763

Gene: PKD1

Linked Data

• gnomAD v4: 16-2114549-C-A
• MyVariant Identifiers: chr16:g.2164550C>A (hg19) ; chr16:g.2114549C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114549C>A , CM000678.2:g.2114549C>A	GRCh38
NC_000016.9:g.2164550C>A , CM000678.1:g.2164550C>A	GRCh37
NC_000016.8:g.2104551C>A	NCBI36
NG_008617.1:g.26350G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2474G>T MANE Select	ENSP00000262304.4:p.Arg825Leu
ENST00000262304.8:c.2474G>T	ENSP00000262304.4:p.Arg825Leu
ENST00000423118.5:c.2474G>T	ENSP00000399501.1:p.Arg825Leu
ENST00000488185.2:c.472+2940G>T
ENST00000568591.5:c.1405G>T	ENSP00000457162.1:n.1405G>T
NM_000296.3:c.2474G>T	NP_000287.3:p.Arg825Leu
NM_001009944.2:c.2474G>T	NP_001009944.2:p.Arg825Leu
XM_011522525.1:c.2528G>T	XP_011520827.1:p.Arg843Leu
XM_011522526.1:c.2528G>T	XP_011520828.1:p.Arg843Leu
XM_011522527.1:c.2528G>T	XP_011520829.1:p.Arg843Leu
XM_011522528.1:c.2528G>T	XP_011520830.1:p.Arg843Leu
XM_011522529.1:c.2528G>T	XP_011520831.1:p.Arg843Leu
XM_011522530.1:c.2474G>T	XP_011520832.1:p.Arg825Leu
XM_011522531.1:c.2456G>T	XP_011520833.1:p.Arg819Leu
XM_011522532.1:c.2402G>T	XP_011520834.1:p.Arg801Leu
XM_011522533.1:c.2321G>T	XP_011520835.1:p.Arg774Leu
XM_011522534.1:c.2264G>T	XP_011520836.1:p.Arg755Leu
XM_011522535.1:c.350G>T	XP_011520837.1:p.Arg117Leu
XM_011522536.1:c.2528G>T	XP_011520838.1:p.Arg843Leu
XR_932867.1:n.2543G>T
XR_932868.1:n.2543G>T
XR_932869.1:n.2543G>T
XR_932870.1:n.2543G>T
XM_005255370.3:c.-576G>T	XP_005255427.1:n.-576G>T
XM_011522528.3:c.2528G>T	XP_011520830.1:p.Arg843Leu
XM_011522529.2:c.2528G>T	XP_011520831.1:p.Arg843Leu
XM_024450298.1:c.2474G>T	XP_024306066.1:p.Arg825Leu
XM_024450299.1:c.2402G>T	XP_024306067.1:p.Arg801Leu
XM_024450300.1:c.2264G>T	XP_024306068.1:p.Arg755Leu
XM_024450301.1:c.350G>T	XP_024306069.1:p.Arg117Leu
NM_000296.4:c.2474G>T	NP_000287.4:p.Arg825Leu
NM_001009944.3:c.2474G>T MANE Select	NP_001009944.3:p.Arg825Leu