Canonical Allele Identifier: CA357619771

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88967991T>A (hg19) ; chr4:g.88046839T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046839T>A , CM000666.2:g.88046839T>A	GRCh38
NC_000004.11:g.88967991T>A , CM000666.1:g.88967991T>A	GRCh37
NC_000004.10:g.89187015T>A	NCBI36
NG_008604.1:g.44172T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1517T>A MANE Select	ENSP00000237596.2:p.Phe506Tyr
ENST00000237596.6:c.1517T>A	ENSP00000237596.2:p.Phe506Tyr
ENST00000508588.5:c.-199+3382T>A	ENSP00000427131.1:n.-199+3382T>A
NM_000297.3:c.1517T>A	NP_000288.1:p.Phe506Tyr
XM_011532028.1:c.1292T>A	XP_011530330.1:p.Phe431Tyr
XM_011532029.1:c.797T>A	XP_011530331.1:p.Phe266Tyr
XM_011532030.1:c.677T>A	XP_011530332.1:p.Phe226Tyr
XR_244632.2:n.1612T>A
NR_156488.1:n.1604T>A
XM_011532028.2:c.1292T>A	XP_011530330.1:p.Phe431Tyr
XM_011532030.2:c.677T>A	XP_011530332.1:p.Phe226Tyr
NM_000297.4:c.1517T>A MANE Select	NP_000288.1:p.Phe506Tyr
NR_156488.2:n.1616T>A