Canonical Allele Identifier: CA2671366549

Gene: PKD2

Linked Data

• gnomAD v4: 4-88046966-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046972dup , CM000666.2:g.88046972dup	GRCh38
NC_000004.11:g.88968124dup , CM000666.1:g.88968124dup	GRCh37
NC_000004.10:g.89187148dup	NCBI36
NG_008604.1:g.44305dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+102dup MANE Select	ENSP00000237596.2:n.1548+102dup
ENST00000237596.6:c.1548+102dup	ENSP00000237596.2:n.1548+102dup
ENST00000508588.5:c.-199+3515dup	ENSP00000427131.1:n.-199+3515dup
NM_000297.3:c.1548+102dup	NP_000288.1:n.1548+102dup
XM_011532028.1:c.1323+102dup	XP_011530330.1:n.1323+102dup
XM_011532029.1:c.828+102dup	XP_011530331.1:n.828+102dup
XM_011532030.1:c.708+102dup	XP_011530332.1:n.708+102dup
XR_244632.2:n.1643+102dup
NR_156488.1:n.1635+102dup
XM_011532028.2:c.1323+102dup	XP_011530330.1:n.1323+102dup
XM_011532030.2:c.708+102dup	XP_011530332.1:n.708+102dup
NM_000297.4:c.1548+102dup MANE Select	NP_000288.1:n.1548+102dup
NR_156488.2:n.1647+102dup