Canonical Allele Identifier: CA357618915

Gene: PKD2

Linked Data

• ClinVar Variation Id: 3066128
• ClinVar RCV Id: RCV003991132
• MyVariant Identifiers: chr4:g.88967869T>A (hg19) ; chr4:g.88046717T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046717T>A , CM000666.2:g.88046717T>A	GRCh38
NC_000004.11:g.88967869T>A , CM000666.1:g.88967869T>A	GRCh37
NC_000004.10:g.89186893T>A	NCBI36
NG_008604.1:g.44050T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1395T>A MANE Select	ENSP00000237596.2:p.Tyr465Ter
ENST00000237596.6:c.1395T>A	ENSP00000237596.2:p.Tyr465Ter
ENST00000508588.5:c.-199+3260T>A	ENSP00000427131.1:n.-199+3260T>A
NM_000297.3:c.1395T>A	NP_000288.1:p.Tyr465Ter
XM_011532028.1:c.1170T>A	XP_011530330.1:p.Tyr390Ter
XM_011532029.1:c.675T>A	XP_011530331.1:p.Tyr225Ter
XM_011532030.1:c.555T>A	XP_011530332.1:p.Tyr185Ter
XR_244632.2:n.1490T>A
NR_156488.1:n.1482T>A
XM_011532028.2:c.1170T>A	XP_011530330.1:p.Tyr390Ter
XM_011532030.2:c.555T>A	XP_011530332.1:p.Tyr185Ter
NM_000297.4:c.1395T>A MANE Select	NP_000288.1:p.Tyr465Ter
NR_156488.2:n.1494T>A