Canonical Allele Identifier: CA493049483

Gene: PKD1

Linked Data

• dbSNP Id: rs1312842468
• gnomAD v2: 16-2164420-G-A
• gnomAD v4: 16-2114419-G-A
• MyVariant Identifiers: chr16:g.2164420G>A (hg19) ; chr16:g.2114419G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114419G>A , CM000678.2:g.2114419G>A	GRCh38
NC_000016.9:g.2164420G>A , CM000678.1:g.2164420G>A	GRCh37
NC_000016.8:g.2104421G>A	NCBI36
NG_008617.1:g.26480C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2604C>T MANE Select	ENSP00000262304.4:p.Ala868=
ENST00000262304.8:c.2604C>T	ENSP00000262304.4:p.Ala868=
ENST00000423118.5:c.2604C>T	ENSP00000399501.1:p.Ala868=
ENST00000488185.2:c.472+3070C>T
ENST00000565639.6:n.63C>T
ENST00000568591.5:c.1535C>T	ENSP00000457162.1:n.1535C>T
NM_000296.3:c.2604C>T	NP_000287.3:p.Ala868=
NM_001009944.2:c.2604C>T	NP_001009944.2:p.Ala868=
XM_011522525.1:c.2658C>T	XP_011520827.1:p.Ala886=
XM_011522526.1:c.2658C>T	XP_011520828.1:p.Ala886=
XM_011522527.1:c.2658C>T	XP_011520829.1:p.Ala886=
XM_011522528.1:c.2658C>T	XP_011520830.1:p.Ala886=
XM_011522529.1:c.2658C>T	XP_011520831.1:p.Ala886=
XM_011522530.1:c.2604C>T	XP_011520832.1:p.Ala868=
XM_011522531.1:c.2586C>T	XP_011520833.1:p.Ala862=
XM_011522532.1:c.2532C>T	XP_011520834.1:p.Ala844=
XM_011522533.1:c.2451C>T	XP_011520835.1:p.Ala817=
XM_011522534.1:c.2394C>T	XP_011520836.1:p.Ala798=
XM_011522535.1:c.480C>T	XP_011520837.1:p.Ala160=
XM_011522536.1:c.2658C>T	XP_011520838.1:p.Ala886=
XR_932867.1:n.2673C>T
XR_932868.1:n.2673C>T
XR_932869.1:n.2673C>T
XR_932870.1:n.2673C>T
XM_005255370.3:c.-446C>T	XP_005255427.1:n.-446C>T
XM_011522528.3:c.2658C>T	XP_011520830.1:p.Ala886=
XM_011522529.2:c.2658C>T	XP_011520831.1:p.Ala886=
XM_024450298.1:c.2604C>T	XP_024306066.1:p.Ala868=
XM_024450299.1:c.2532C>T	XP_024306067.1:p.Ala844=
XM_024450300.1:c.2394C>T	XP_024306068.1:p.Ala798=
XM_024450301.1:c.480C>T	XP_024306069.1:p.Ala160=
NM_000296.4:c.2604C>T	NP_000287.4:p.Ala868=
NM_001009944.3:c.2604C>T MANE Select	NP_001009944.3:p.Ala868=