Canonical Allele Identifier: CA1065137046

Gene: PKD2

Linked Data

• dbSNP Id: rs1727800644
• gnomAD v3: 4-88047031-G-T
• gnomAD v4: 4-88047031-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88047031G>T , CM000666.2:g.88047031G>T	GRCh38
NC_000004.11:g.88968183G>T , CM000666.1:g.88968183G>T	GRCh37
NC_000004.10:g.89187207G>T	NCBI36
NG_008604.1:g.44364G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+161G>T MANE Select	ENSP00000237596.2:n.1548+161G>T
ENST00000237596.6:c.1548+161G>T	ENSP00000237596.2:n.1548+161G>T
ENST00000508588.5:c.-199+3574G>T	ENSP00000427131.1:n.-199+3574G>T
NM_000297.3:c.1548+161G>T	NP_000288.1:n.1548+161G>T
XM_011532028.1:c.1323+161G>T	XP_011530330.1:n.1323+161G>T
XM_011532029.1:c.828+161G>T	XP_011530331.1:n.828+161G>T
XM_011532030.1:c.708+161G>T	XP_011530332.1:n.708+161G>T
XR_244632.2:n.1643+161G>T
NR_156488.1:n.1635+161G>T
XM_011532028.2:c.1323+161G>T	XP_011530330.1:n.1323+161G>T
XM_011532030.2:c.708+161G>T	XP_011530332.1:n.708+161G>T
NM_000297.4:c.1548+161G>T MANE Select	NP_000288.1:n.1548+161G>T
NR_156488.2:n.1647+161G>T