Canonical Allele Identifier: CA2671365786

Gene: PKD2

Linked Data

• gnomAD v4: 4-88038215-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038215T>C , CM000666.2:g.88038215T>C	GRCh38
NC_000004.11:g.88959367T>C , CM000666.1:g.88959367T>C	GRCh37
NC_000004.10:g.89178391T>C	NCBI36
NG_008604.1:g.35548T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.844-36T>C MANE Select	ENSP00000237596.2:n.844-36T>C
ENST00000237596.6:c.844-36T>C	ENSP00000237596.2:n.844-36T>C
ENST00000506367.1:n.291-36T>C
ENST00000506727.1:n.430-36T>C
NM_000297.3:c.844-36T>C	NP_000288.1:n.844-36T>C
XM_011532028.1:c.844-36T>C	XP_011530330.1:n.844-36T>C
XM_011532029.1:c.124-36T>C	XP_011530331.1:n.124-36T>C
XM_011532030.1:c.4-36T>C	XP_011530332.1:n.4-36T>C
XR_244632.2:n.939-36T>C
NR_156488.1:n.931-36T>C
XM_011532028.2:c.844-36T>C	XP_011530330.1:n.844-36T>C
XM_011532030.2:c.4-36T>C	XP_011530332.1:n.4-36T>C
NM_000297.4:c.844-36T>C MANE Select	NP_000288.1:n.844-36T>C
NR_156488.2:n.943-36T>C