Canonical Allele Identifier: CA1931710320
Gene: PKD2L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100315676G= , CM000672.2:g.100315676G= GRCh38
NC_000010.10:g.102075433G= , CM000672.1:g.102075433G= GRCh37
NC_000010.9:g.102065423G= NCBI36
NG_047099.1:g.35849C=

Transcript Alleles

HGVS Amino-acid change
ENST00000318222.4:c.349+13535C= MANE Select ENSP00000325296.3:n.349+13535C=
ENST00000318222.3:c.349+13535C= ENSP00000325296.3:n.349+13535C=
ENST00000465680.2:c.104+14193C=
ENST00000528248.1:c.208+13535C=
ENST00000532547.1:c.*93+13535C= ENSP00000434224.1:n.*93+13535C=
NM_001253837.1:c.208+13535C= NP_001240766.1:n.208+13535C=
NM_016112.2:c.349+13535C= NP_057196.2:n.349+13535C=
XM_011540321.1:c.349+13535C= XP_011538623.1:n.349+13535C=
XM_011540322.1:c.349+13535C= XP_011538624.1:n.349+13535C=
XM_011540323.1:c.59-15958C= XP_011538625.1:n.59-15958C=
XM_011540324.1:c.59-15958C= XP_011538626.1:n.59-15958C=
XM_011540325.1:c.-11-15958C= XP_011538627.1:n.-11-15958C=
XR_945861.1:n.622+13535C=
XM_011540323.3:c.59-15958C= XP_011538625.1:n.59-15958C=
XM_011540325.3:c.-11-15958C= XP_011538627.1:n.-11-15958C=
XM_017016875.2:c.59-15958C= XP_016872364.1:n.59-15958C=
XM_017016876.1:c.101-15958C= XP_016872365.1:n.101-15958C=
NM_016112.3:c.349+13535C= MANE Select NP_057196.2:n.349+13535C=
NM_001253837.2:c.208+13535C= NP_001240766.1:n.208+13535C=