Canonical Allele Identifier: CA1474562208

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88007868_88007943delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA , CM000666.2:g.88007868_88007943delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA	GRCh38
NC_000004.11:g.88929020_88929095delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA , CM000666.1:g.88929020_88929095delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA	GRCh37
NC_000004.10:g.89148044_89148119delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA	NCBI36
NG_008604.1:g.5201_5276delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.135_210delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA MANE Select	ENSP00000237596.2:p.Gly45=
ENST00000237596.6:c.135_210delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA	ENSP00000237596.2:p.Gly45=
NM_000297.3:c.135_210delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA	NP_000288.1:p.Gly45=
XM_011532028.1:c.135_210delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA	XP_011530330.1:p.Gly45=
XR_244632.2:n.230_305delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA
NR_156488.1:n.222_297delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA
XM_011532028.2:c.135_210delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA	XP_011530330.1:p.Gly45=
NM_000297.4:c.135_210delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA MANE Select	NP_000288.1:p.Gly45=
NR_156488.2:n.234_309delinsCCTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA