Canonical Allele Identifier: CA917247595

Gene: PKD2

Linked Data

• dbSNP Id: rs1578136111

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046917_88046918insA , CM000666.2:g.88046917_88046918insA	GRCh38
NC_000004.11:g.88968069_88968070insA , CM000666.1:g.88968069_88968070insA	GRCh37
NC_000004.10:g.89187093_89187094insA	NCBI36
NG_008604.1:g.44250_44251insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+47_1548+48insA MANE Select	ENSP00000237596.2:n.1548+47_1548+48insA
ENST00000237596.6:c.1548+47_1548+48insA	ENSP00000237596.2:n.1548+47_1548+48insA
ENST00000508588.5:c.-199+3460_-199+3461insA	ENSP00000427131.1:n.-199+3460_-199+3461insA
NM_000297.3:c.1548+47_1548+48insA	NP_000288.1:n.1548+47_1548+48insA
XM_011532028.1:c.1323+47_1323+48insA	XP_011530330.1:n.1323+47_1323+48insA
XM_011532029.1:c.828+47_828+48insA	XP_011530331.1:n.828+47_828+48insA
XM_011532030.1:c.708+47_708+48insA	XP_011530332.1:n.708+47_708+48insA
XR_244632.2:n.1643+47_1643+48insA
NR_156488.1:n.1635+47_1635+48insA
XM_011532028.2:c.1323+47_1323+48insA	XP_011530330.1:n.1323+47_1323+48insA
XM_011532030.2:c.708+47_708+48insA	XP_011530332.1:n.708+47_708+48insA
NM_000297.4:c.1548+47_1548+48insA MANE Select	NP_000288.1:n.1548+47_1548+48insA
NR_156488.2:n.1647+47_1647+48insA