Canonical Allele Identifier: CA2671366568

Gene: PKD2

Linked Data

• gnomAD v4: 4-88046997-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046997T>C , CM000666.2:g.88046997T>C	GRCh38
NC_000004.11:g.88968149T>C , CM000666.1:g.88968149T>C	GRCh37
NC_000004.10:g.89187173T>C	NCBI36
NG_008604.1:g.44330T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+127T>C MANE Select	ENSP00000237596.2:n.1548+127T>C
ENST00000237596.6:c.1548+127T>C	ENSP00000237596.2:n.1548+127T>C
ENST00000508588.5:c.-199+3540T>C	ENSP00000427131.1:n.-199+3540T>C
NM_000297.3:c.1548+127T>C	NP_000288.1:n.1548+127T>C
XM_011532028.1:c.1323+127T>C	XP_011530330.1:n.1323+127T>C
XM_011532029.1:c.828+127T>C	XP_011530331.1:n.828+127T>C
XM_011532030.1:c.708+127T>C	XP_011530332.1:n.708+127T>C
XR_244632.2:n.1643+127T>C
NR_156488.1:n.1635+127T>C
XM_011532028.2:c.1323+127T>C	XP_011530330.1:n.1323+127T>C
XM_011532030.2:c.708+127T>C	XP_011530332.1:n.708+127T>C
NM_000297.4:c.1548+127T>C MANE Select	NP_000288.1:n.1548+127T>C
NR_156488.2:n.1647+127T>C