Canonical Allele Identifier: CA2671370599

Gene: PKD2

Linked Data

• gnomAD v4: 4-88065536-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065536T>A , CM000666.2:g.88065536T>A	GRCh38
NC_000004.11:g.88986688T>A , CM000666.1:g.88986688T>A	GRCh37
NC_000004.10:g.89205712T>A	NCBI36
NG_008604.1:g.62869T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2240+41T>A MANE Select	ENSP00000237596.2:n.2240+41T>A
ENST00000237596.6:c.2240+41T>A	ENSP00000237596.2:n.2240+41T>A
ENST00000502363.1:c.494+41T>A	ENSP00000425289.1:n.494+41T>A
ENST00000508588.5:c.494+41T>A	ENSP00000427131.1:n.494+41T>A
ENST00000511337.5:n.492+41T>A
ENST00000512858.1:n.493T>A
NM_000297.3:c.2240+41T>A	NP_000288.1:n.2240+41T>A
XM_011532028.1:c.2015+41T>A	XP_011530330.1:n.2015+41T>A
XM_011532029.1:c.1520+41T>A	XP_011530331.1:n.1520+41T>A
XM_011532030.1:c.1400+41T>A	XP_011530332.1:n.1400+41T>A
NR_156488.1:n.2206+41T>A
XM_011532028.2:c.2015+41T>A	XP_011530330.1:n.2015+41T>A
XM_011532030.2:c.1400+41T>A	XP_011530332.1:n.1400+41T>A
NM_000297.4:c.2240+41T>A MANE Select	NP_000288.1:n.2240+41T>A
NR_156488.2:n.2218+41T>A