Canonical Allele Identifier: CA394387366

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2164421G>T (hg19) ; chr16:g.2114420G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114420G>T , CM000678.2:g.2114420G>T	GRCh38
NC_000016.9:g.2164421G>T , CM000678.1:g.2164421G>T	GRCh37
NC_000016.8:g.2104422G>T	NCBI36
NG_008617.1:g.26479C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2603C>A MANE Select	ENSP00000262304.4:p.Ala868Asp
ENST00000262304.8:c.2603C>A	ENSP00000262304.4:p.Ala868Asp
ENST00000423118.5:c.2603C>A	ENSP00000399501.1:p.Ala868Asp
ENST00000488185.2:c.472+3069C>A
ENST00000565639.6:n.62C>A
ENST00000568591.5:c.1534C>A	ENSP00000457162.1:n.1534C>A
NM_000296.3:c.2603C>A	NP_000287.3:p.Ala868Asp
NM_001009944.2:c.2603C>A	NP_001009944.2:p.Ala868Asp
XM_011522525.1:c.2657C>A	XP_011520827.1:p.Ala886Asp
XM_011522526.1:c.2657C>A	XP_011520828.1:p.Ala886Asp
XM_011522527.1:c.2657C>A	XP_011520829.1:p.Ala886Asp
XM_011522528.1:c.2657C>A	XP_011520830.1:p.Ala886Asp
XM_011522529.1:c.2657C>A	XP_011520831.1:p.Ala886Asp
XM_011522530.1:c.2603C>A	XP_011520832.1:p.Ala868Asp
XM_011522531.1:c.2585C>A	XP_011520833.1:p.Ala862Asp
XM_011522532.1:c.2531C>A	XP_011520834.1:p.Ala844Asp
XM_011522533.1:c.2450C>A	XP_011520835.1:p.Ala817Asp
XM_011522534.1:c.2393C>A	XP_011520836.1:p.Ala798Asp
XM_011522535.1:c.479C>A	XP_011520837.1:p.Ala160Asp
XM_011522536.1:c.2657C>A	XP_011520838.1:p.Ala886Asp
XR_932867.1:n.2672C>A
XR_932868.1:n.2672C>A
XR_932869.1:n.2672C>A
XR_932870.1:n.2672C>A
XM_005255370.3:c.-447C>A	XP_005255427.1:n.-447C>A
XM_011522528.3:c.2657C>A	XP_011520830.1:p.Ala886Asp
XM_011522529.2:c.2657C>A	XP_011520831.1:p.Ala886Asp
XM_024450298.1:c.2603C>A	XP_024306066.1:p.Ala868Asp
XM_024450299.1:c.2531C>A	XP_024306067.1:p.Ala844Asp
XM_024450300.1:c.2393C>A	XP_024306068.1:p.Ala798Asp
XM_024450301.1:c.479C>A	XP_024306069.1:p.Ala160Asp
NM_000296.4:c.2603C>A	NP_000287.4:p.Ala868Asp
NM_001009944.3:c.2603C>A MANE Select	NP_001009944.3:p.Ala868Asp