Canonical Allele Identifier: CA2671366562

Gene: PKD2

Linked Data

• gnomAD v4: 4-88046988-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046988C>A , CM000666.2:g.88046988C>A	GRCh38
NC_000004.11:g.88968140C>A , CM000666.1:g.88968140C>A	GRCh37
NC_000004.10:g.89187164C>A	NCBI36
NG_008604.1:g.44321C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+118C>A MANE Select	ENSP00000237596.2:n.1548+118C>A
ENST00000237596.6:c.1548+118C>A	ENSP00000237596.2:n.1548+118C>A
ENST00000508588.5:c.-199+3531C>A	ENSP00000427131.1:n.-199+3531C>A
NM_000297.3:c.1548+118C>A	NP_000288.1:n.1548+118C>A
XM_011532028.1:c.1323+118C>A	XP_011530330.1:n.1323+118C>A
XM_011532029.1:c.828+118C>A	XP_011530331.1:n.828+118C>A
XM_011532030.1:c.708+118C>A	XP_011530332.1:n.708+118C>A
XR_244632.2:n.1643+118C>A
NR_156488.1:n.1635+118C>A
XM_011532028.2:c.1323+118C>A	XP_011530330.1:n.1323+118C>A
XM_011532030.2:c.708+118C>A	XP_011530332.1:n.708+118C>A
NM_000297.4:c.1548+118C>A MANE Select	NP_000288.1:n.1548+118C>A
NR_156488.2:n.1647+118C>A