Canonical Allele Identifier: CA357619406

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88967933T>A (hg19) ; chr4:g.88046781T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046781T>A , CM000666.2:g.88046781T>A	GRCh38
NC_000004.11:g.88967933T>A , CM000666.1:g.88967933T>A	GRCh37
NC_000004.10:g.89186957T>A	NCBI36
NG_008604.1:g.44114T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1459T>A MANE Select	ENSP00000237596.2:p.Tyr487Asn
ENST00000237596.6:c.1459T>A	ENSP00000237596.2:p.Tyr487Asn
ENST00000508588.5:c.-199+3324T>A	ENSP00000427131.1:n.-199+3324T>A
NM_000297.3:c.1459T>A	NP_000288.1:p.Tyr487Asn
XM_011532028.1:c.1234T>A	XP_011530330.1:p.Tyr412Asn
XM_011532029.1:c.739T>A	XP_011530331.1:p.Tyr247Asn
XM_011532030.1:c.619T>A	XP_011530332.1:p.Tyr207Asn
XR_244632.2:n.1554T>A
NR_156488.1:n.1546T>A
XM_011532028.2:c.1234T>A	XP_011530330.1:p.Tyr412Asn
XM_011532030.2:c.619T>A	XP_011530332.1:p.Tyr207Asn
NM_000297.4:c.1459T>A MANE Select	NP_000288.1:p.Tyr487Asn
NR_156488.2:n.1558T>A