Canonical Allele Identifier: CA357618897

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88967867T>A (hg19) ; chr4:g.88046715T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046715T>A , CM000666.2:g.88046715T>A	GRCh38
NC_000004.11:g.88967867T>A , CM000666.1:g.88967867T>A	GRCh37
NC_000004.10:g.89186891T>A	NCBI36
NG_008604.1:g.44048T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1393T>A MANE Select	ENSP00000237596.2:p.Tyr465Asn
ENST00000237596.6:c.1393T>A	ENSP00000237596.2:p.Tyr465Asn
ENST00000508588.5:c.-199+3258T>A	ENSP00000427131.1:n.-199+3258T>A
NM_000297.3:c.1393T>A	NP_000288.1:p.Tyr465Asn
XM_011532028.1:c.1168T>A	XP_011530330.1:p.Tyr390Asn
XM_011532029.1:c.673T>A	XP_011530331.1:p.Tyr225Asn
XM_011532030.1:c.553T>A	XP_011530332.1:p.Tyr185Asn
XR_244632.2:n.1488T>A
NR_156488.1:n.1480T>A
XM_011532028.2:c.1168T>A	XP_011530330.1:p.Tyr390Asn
XM_011532030.2:c.553T>A	XP_011530332.1:p.Tyr185Asn
NM_000297.4:c.1393T>A MANE Select	NP_000288.1:p.Tyr465Asn
NR_156488.2:n.1492T>A