Canonical Allele Identifier: CA1474579545
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88046636A= , CM000666.2:g.88046636A= GRCh38
NC_000004.11:g.88967788A= , CM000666.1:g.88967788A= GRCh37
NC_000004.10:g.89186812A= NCBI36
NG_008604.1:g.43969A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1320-6A= MANE Select ENSP00000237596.2:n.1320-6A=
ENST00000237596.6:c.1320-6A= ENSP00000237596.2:n.1320-6A=
ENST00000508588.5:c.-199+3179A= ENSP00000427131.1:n.-199+3179A=
NM_000297.3:c.1320-6A= NP_000288.1:n.1320-6A=
XM_011532028.1:c.1095-6A= XP_011530330.1:n.1095-6A=
XM_011532029.1:c.600-6A= XP_011530331.1:n.600-6A=
XM_011532030.1:c.480-6A= XP_011530332.1:n.480-6A=
XR_244632.2:n.1415-6A=
NR_156488.1:n.1407-6A=
XM_011532028.2:c.1095-6A= XP_011530330.1:n.1095-6A=
XM_011532030.2:c.480-6A= XP_011530332.1:n.480-6A=
NM_000297.4:c.1320-6A= MANE Select NP_000288.1:n.1320-6A=
NR_156488.2:n.1419-6A=