Canonical Allele Identifier: CA394389716
Gene: PKD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2115474A>T , CM000678.2:g.2115474A>T GRCh38
NC_000016.9:g.2165475A>T , CM000678.1:g.2165475A>T GRCh37
NC_000016.8:g.2105476A>T NCBI36
NG_008617.1:g.25425T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.2001T>A MANE Select ENSP00000262304.4:p.Asn667Lys
ENST00000262304.8:c.2001T>A ENSP00000262304.4:p.Asn667Lys
ENST00000423118.5:c.2001T>A ENSP00000399501.1:p.Asn667Lys
ENST00000488185.2:c.472+2015T>A
ENST00000568591.5:c.932T>A ENSP00000457162.1:n.932T>A
NM_000296.3:c.2001T>A NP_000287.3:p.Asn667Lys
NM_001009944.2:c.2001T>A NP_001009944.2:p.Asn667Lys
XM_011522525.1:c.2055T>A XP_011520827.1:p.Asn685Lys
XM_011522526.1:c.2055T>A XP_011520828.1:p.Asn685Lys
XM_011522527.1:c.2055T>A XP_011520829.1:p.Asn685Lys
XM_011522528.1:c.2055T>A XP_011520830.1:p.Asn685Lys
XM_011522529.1:c.2055T>A XP_011520831.1:p.Asn685Lys
XM_011522530.1:c.2001T>A XP_011520832.1:p.Asn667Lys
XM_011522531.1:c.1983T>A XP_011520833.1:p.Asn661Lys
XM_011522532.1:c.1929T>A XP_011520834.1:p.Asn643Lys
XM_011522533.1:c.1848T>A XP_011520835.1:p.Asn616Lys
XM_011522534.1:c.1791T>A XP_011520836.1:p.Asn597Lys
XM_011522536.1:c.2055T>A XP_011520838.1:p.Asn685Lys
XR_932867.1:n.2070T>A
XR_932868.1:n.2070T>A
XR_932869.1:n.2070T>A
XR_932870.1:n.2070T>A
XM_011522528.3:c.2055T>A XP_011520830.1:p.Asn685Lys
XM_011522529.2:c.2055T>A XP_011520831.1:p.Asn685Lys
XM_024450298.1:c.2001T>A XP_024306066.1:p.Asn667Lys
XM_024450299.1:c.1929T>A XP_024306067.1:p.Asn643Lys
XM_024450300.1:c.1791T>A XP_024306068.1:p.Asn597Lys
NM_000296.4:c.2001T>A NP_000287.4:p.Asn667Lys
NM_001009944.3:c.2001T>A MANE Select NP_001009944.3:p.Asn667Lys